- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00296036
Pyridoxine and Topical Urea/Lactic Acid-Based Cream in Preventing Hand-Foot Syndrome in Patients Receiving Capecitabine for Breast Cancer or Other Cancer
A Phase III Randomized, Placebo-controlled, Double-blind Trial to Determine the Effectiveness of a Urea/Lactic Acid-Based Topical Keratolytic Agent and Vitamin B-6 for Prevention of Capecitabine-Induced Hand and Foot Syndrome
RATIONALE: Pyridoxine (vitamin B6) and topical urea/lactic acid-based cream may prevent or lessen hand-foot syndrome caused by chemotherapy. It is not yet known whether giving pyridoxine with or without topical urea/lactic acid-based cream is more effective than topical urea/lactic acid-based cream alone or a placebo in preventing hand-foot syndrome.
PURPOSE: This randomized phase III trial is studying pyridoxine and topical urea/lactic acid-based cream to see how well they work compared with giving pyridoxine together with a placebo, giving topical urea/lactic acid-based cream together with a placebo, or giving two placebos in preventing hand-foot syndrome in patients who are receiving capecitabine for breast cancer or other cancer.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
OBJECTIVES:
- Determine whether the prophylactic use of a topical urea/lactic acid cream can decrease the incidence/severity of capecitabine-caused palmar-plantar erythrodysesthesia in patients receiving capecitabine for breast and/or other cancer.
- Evaluate the potential toxicity of this cream.
- Determine whether the prophylactic use of vitamin B6 can decrease the incidence and/or severity of capecitabine-caused palmar-plantar erythrodysesthesia.
- Evaluate the potential toxicity of vitamin B6.
- Determine whether the prophylactic use of a topical urea/lactic acid cream in combination with vitamin B6 can decrease the incidence and/or severity of capecitabine caused palmar-plantar erythrodysesthesia.
OUTLINE: This is a randomized, double-blind, placebo-controlled study. Patients are stratified according to age (< 50 years old vs 50-60 years old vs > 60 years old), sex, capecitabine dose level (2000 mg/day vs 2500 mg/day), cancer type (breast vs other), and mode of therapy (adjuvant [including neo-adjuvant] therapy vs metastatic disease). Patients are randomized to 1 of 6 treatment arms (treatment arms I-IV closed to accrual as of 10/24/007).
- Arm I (closed to accrual as of 10/24/2007): Patients receive topical urea/lactic acid-based cream applied to palms and soles twice daily and oral pyridoxine once daily on days 1-21.
- Arm II (closed to accrual as of 10/24/2007): Patients receive topical urea/lactic acid-based cream as in arm I (closed to accrual as of 10/24/2007) and oral placebo once daily on days 1-21.
- Arm III (closed to accrual as of 10/24/2007): Patients receive placebo cream applied to palms and soles twice daily and pyridoxine as in arm I (closed to accrual as of 10/24/2007).
- Arm IV (closed to accrual as of 10/24/2007):Patients receive placebo cream as in arm III and oral placebo as in arm II (closed to accrual as of 10/24/2007).
- Arm V: Patients receive topical urea/lactic acid-based cream applied to palms and soles twice daily on days 1-21.
- Arm VI: Patients receive placebo cream applied to palms and soles twice daily on days 1-21.
In all arms, treatment repeats every 21 days for up to 4 courses in the absence of disease progression or unacceptable toxicity.
Study Type
Enrollment (Actual)
Phase
- Phase 3
Contacts and Locations
Study Locations
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Arizona
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Scottsdale, Arizona, United States, 85259-5499
- Mayo Clinic Scottsdale
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Colorado
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Aurora, Colorado, United States, 80012
- Aurora Presbyterian Hospital
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Boulder, Colorado, United States, 80301-9019
- Boulder Community Hospital
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Colorado Springs, Colorado, United States, 80933
- Penrose Cancer Center at Penrose Hospital
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Denver, Colorado, United States, 80210
- Porter Adventist Hospital
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Denver, Colorado, United States, 80220
- Rose Medical Center
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Denver, Colorado, United States, 80218
- Presbyterian - St. Luke's Medical Center
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Denver, Colorado, United States, 80204
- St. Anthony Central Hospital
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Denver, Colorado, United States, 80218
- St. Joseph Hospital
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Denver, Colorado, United States, 80224-2522
- CCOP - Colorado Cancer Research Program
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Englewood, Colorado, United States, 80110
- Swedish Medical Center
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Grand Junction, Colorado, United States, 81502
- St. Mary's Regional Cancer Center at St. Mary's Hospital and Medical Center
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Greeley, Colorado, United States, 80631
- North Colorado Medical Center
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Lone Tree, Colorado, United States, 80124
- Sky Ridge Medical Center
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Longmont, Colorado, United States, 80502
- Hope Cancer Care Center at Longmont United Hospital
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Loveland, Colorado, United States, 80539
- McKee Medical Center
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Pueblo, Colorado, United States, 81004
- St. Mary - Corwin Regional Medical Center
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Thornton, Colorado, United States, 80229
- North Suburban Medical Center
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Wheat Ridge, Colorado, United States, 80033
- Exempla Lutheran Medical Center
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Florida
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Hollywood, Florida, United States, 33021
- Memorial Cancer Institute at Memorial Regional Hospital
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Jacksonville, Florida, United States, 32224
- Mayo Clinic - Jacksonville
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Illinois
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Aurora, Illinois, United States, 60504
- Rush-Copley Cancer Care Center
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Bloomington, Illinois, United States, 61701
- St. Joseph Medical Center
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Canton, Illinois, United States, 61520
- Graham Hospital
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Carthage, Illinois, United States, 62321
- Memorial Hospital
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Eureka, Illinois, United States, 61530
- Eureka Community Hospital
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Galesburg, Illinois, United States, 61401
- Galesburg Cottage Hospital
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Galesburg, Illinois, United States, 61401
- Galesburg Clinic, PC
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Havana, Illinois, United States, 62644
- Mason District Hospital
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Hopedale, Illinois, United States, 61747
- Hopedale Medical Complex
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Joliet, Illinois, United States, 60435
- Joliet Oncology-Hematology Associates, Limited - West
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Macomb, Illinois, United States, 61455
- Mcdonough District Hospital
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Moline, Illinois, United States, 61265
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Moline, Illinois, United States, 61265
- Trinity Cancer Center at Trinity Medical Center - 7th Street Campus
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Normal, Illinois, United States, 61761
- Bromenn Regional Medical Center
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Normal, Illinois, United States, 61761
- Community Cancer Center
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Ottawa, Illinois, United States, 61350
- Community Hospital of Ottawa
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Ottawa, Illinois, United States, 61350
- Oncology Hematology Associates of Central Illinois, PC - Ottawa
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Pekin, Illinois, United States, 61554
- Cancer Treatment Center at Pekin Hospital
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Peoria, Illinois, United States, 61636
- Methodist Medical Center of Illinois
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Peoria, Illinois, United States, 61614
- Proctor Hospital
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Peoria, Illinois, United States, 61637
- OSF St. Francis Medical Center
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Peoria, Illinois, United States, 61615
- CCOP - Illinois Oncology Research Association
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Peoria, Illinois, United States, 61615
- Oncology Hematology Associates of Central Illinois, PC - Peoria
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Peru, Illinois, United States, 61354
- Illinois Valley Community Hospital
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Princeton, Illinois, United States, 61356
- Perry Memorial Hospital
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Spring Valley, Illinois, United States, 61362
- St. Margaret's Hospital
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Urbana, Illinois, United States, 61801
- Carle Cancer Center at Carle Foundation Hospital
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Urbana, Illinois, United States, 61801
- CCOP - Carle Cancer Center
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Indiana
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Beech Grove, Indiana, United States, 46107
- St. Francis Hospital and Health Centers - Beech Grove Campus
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Elkhart, Indiana, United States, 46515
- Elkhart General Hospital
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Kokomo, Indiana, United States, 46904
- Howard Community Hospital
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Michigan City, Indiana, United States, 46360
- Saint Anthony Memorial Health Centers
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Richmond, Indiana, United States, 47374
- Reid Hospital & Health Care Services
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South Bend, Indiana, United States, 46601
- Memorial Hospital of South Bend
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South Bend, Indiana, United States, 46601
- CCOP - Northern Indiana CR Consortium
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South Bend, Indiana, United States, 46617
- Saint Joseph Regional Medical Center
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South Bend, Indiana, United States, 46617
- South Bend Clinic
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Iowa
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Ames, Iowa, United States, 50010
- McFarland Clinic, PC
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Bettendorf, Iowa, United States, 52722
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Cedar Rapids, Iowa, United States, 52403
- Cedar Rapids Oncology Associates
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Cedar Rapids, Iowa, United States, 52403
- Mercy Regional Cancer Center at Mercy Medical Center
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Des Moines, Iowa, United States, 50309
- CCOP - Iowa Oncology Research Association
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Des Moines, Iowa, United States, 50309
- John Stoddard Cancer Center at Iowa Methodist Medical Center
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Des Moines, Iowa, United States, 50309
- Medical Oncology and Hematology Associates at John Stoddard Cancer Center
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Des Moines, Iowa, United States, 50314
- Medical Oncology and Hematology Associates at Mercy Cancer Center
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Des Moines, Iowa, United States, 50314
- Mercy Cancer Center at Mercy Medical Center - Des Moines
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Des Moines, Iowa, United States, 50316
- John Stoddard Cancer Center at Iowa Lutheran Hospital
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Des Moines, Iowa, United States, 50307
- Mercy Capitol Hospital
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Ottumwa, Iowa, United States, 52501
- McCreery Cancer Center at Ottumwa Regional
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Sioux City, Iowa, United States, 51101
- Siouxland Hematology-Oncology Associates, LLP
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Sioux City, Iowa, United States, 51104
- St. Luke's Regional Medical Center
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Sioux City, Iowa, United States, 51104
- Mercy Medical Center - Sioux City
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Kansas
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Chanute, Kansas, United States, 66720
- Cancer Center of Kansas, PA - Chanute
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Dodge City, Kansas, United States, 67801
- Cancer Center of Kansas, PA - Dodge City
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El Dorado, Kansas, United States, 67042
- Cancer Center of Kansas, PA - El Dorado
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Independence, Kansas, United States, 67301
- Cancer Center of Kansas-Independence
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Kingman, Kansas, United States, 67068
- Cancer Center of Kansas, PA - Kingman
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Liberal, Kansas, United States, 67901
- Southwest Medical Center
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Newton, Kansas, United States, 67114
- Cancer Center of Kansas, PA - Newton
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Parsons, Kansas, United States, 67357
- Cancer Center of Kansas, PA - Parsons
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Pratt, Kansas, United States, 67124
- Cancer Center of Kansas, PA - Pratt
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Salina, Kansas, United States, 67042
- Cancer Center of Kansas, PA - Salina
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Wellington, Kansas, United States, 67152
- Cancer Center of Kansas, PA - Wellington
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Wichita, Kansas, United States, 67208
- Cancer Center of Kansas, PA - Medical Arts Tower
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Wichita, Kansas, United States, 67214
- Cancer Center of Kansas, PA - Wichita
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Wichita, Kansas, United States, 67214
- CCOP - Wichita
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Wichita, Kansas, United States, 67214
- Via Christi Cancer Center at Via Christi Regional Medical Center
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Wichita, Kansas, United States, 67208
- Associates in Womens Health, PA - North Review
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Winfield, Kansas, United States, 67156
- Cancer Center of Kansas, PA - Winfield
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Michigan
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Adrian, Michigan, United States, 49221
- Hickman Cancer Center at Bixby Medical Center
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Ann Arbor, Michigan, United States, 48106-0995
- Saint Joseph Mercy Cancer Center
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Ann Arbor, Michigan, United States, 48106
- CCOP - Michigan Cancer Research Consortium
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Dearborn, Michigan, United States, 48123-2500
- Oakwood Cancer Center at Oakwood Hospital and Medical Center
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Escanaba, Michigan, United States, 49431
- Green Bay Oncology, Limited - Escanaba
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Flint, Michigan, United States, 48503
- Hurley Medical Center
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Flint, Michigan, United States, 48503
- Genesys Hurley Cancer Institute
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Grosse Pointe Woods, Michigan, United States, 48236
- Van Elslander Cancer Center at St. John Hospital and Medical Center
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Iron Mountain, Michigan, United States, 49801
- Dickinson County Healthcare System
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Jackson, Michigan, United States, 49201
- Foote Memorial Hospital
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Lambertville, Michigan, United States, 48144
- Haematology-Oncology Associates of Ohio and Michigan, PC
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Lansing, Michigan, United States, 48912-1811
- Sparrow Regional Cancer Center
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Livonia, Michigan, United States, 48154
- St. Mary Mercy Hospital
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Monroe, Michigan, United States, 48162
- Community Cancer Center of Monroe
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Monroe, Michigan, United States, 48162
- Mercy Memorial Hospital - Monroe
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Pontiac, Michigan, United States, 48341-2985
- St. Joseph Mercy Oakland
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Port Huron, Michigan, United States, 48060
- Mercy Regional Cancer Center at Mercy Hospital
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Saginaw, Michigan, United States, 48601
- Seton Cancer Institute at Saint Mary's - Saginaw
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St. Joseph, Michigan, United States, 49085
- Lakeland Regional Cancer Care Center - St. Joseph
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Warren, Michigan, United States, 48093
- St. John Macomb Hospital
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Minnesota
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Albert Lea, Minnesota, United States, 56007
- Albert Lea Cancer Center at Albert Lea Medical Center
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Alexandria, Minnesota, United States, 56308
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Bemidji, Minnesota, United States, 56601
- MeritCare Bemidji
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Burnsville, Minnesota, United States, 55337
- Fairview Ridges Hospital
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Coon Rapids, Minnesota, United States, 55433
- Mercy and Unity Cancer Center at Mercy Hospital
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Duluth, Minnesota, United States, 55805
- CCOP - Duluth
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Duluth, Minnesota, United States, 55805-1983
- Duluth Clinic Cancer Center - Duluth
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Duluth, Minnesota, United States, 55805
- Miller - Dwan Medical Center
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Edina, Minnesota, United States, 55435
- Fairview Southdale Hospital
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Fergus Falls, Minnesota, United States, 56537
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Fridley, Minnesota, United States, 55432
- Mercy and Unity Cancer Center at Unity Hospital
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Hutchinson, Minnesota, United States, 55350
- Hutchinson Area Health Care
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Lichfield, Minnesota, United States, 55355
- Meeker County Memorial Hospital
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Mankato, Minnesota, United States, 56002
- Immanuel St. Joseph's
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Maplewood, Minnesota, United States, 55109
- Minnesota Oncology Hematology, PA - Maplewood
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Maplewood, Minnesota, United States, 55109
- HealthEast Cancer Care at St. John's Hospital
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Minneapolis, Minnesota, United States, 55407
- Virginia Piper Cancer Institute at Abbott - Northwestern Hospital
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Minneapolis, Minnesota, United States, 55415
- Hennepin County Medical Center - Minneapolis
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Robbinsdale, Minnesota, United States, 55422-2900
- Hubert H. Humphrey Cancer Center at North Memorial Outpatient Center
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Rochester, Minnesota, United States, 55905
- Mayo Clinic Cancer Center
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Saint Cloud, Minnesota, United States, 56303
- CentraCare Clinic - River Campus
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Saint Cloud, Minnesota, United States, 56303
- Coborn Cancer Center
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Saint Louis Park, Minnesota, United States, 55416
- CCOP - Metro-Minnesota
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Saint Louis Park, Minnesota, United States, 55416
- Park Nicollet Cancer Center
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Saint Paul, Minnesota, United States, 55102
- United Hospital
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Saint Paul, Minnesota, United States, 55102
- HealthEast Cancer Care at St. Joseph's Hospital
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Shakopee, Minnesota, United States, 55379
- St. Francis Cancer Center at St. Francis Medical Center
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St. Paul, Minnesota, United States, 55101
- Regions Hospital Cancer Care Center
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Waconia, Minnesota, United States, 55387
- Ridgeview Medical Center
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Woodbury, Minnesota, United States, 55125
- Minnesota Oncology Hematology, PA - Woodbury
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Woodbury, Minnesota, United States, 55125
- HealthEast Cancer Care at Woodwinds Health Campus
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Missouri
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Saint Louis, Missouri, United States, 63131
- Missouri Baptist Cancer Center
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Saint Louis, Missouri, United States, 63141
- Arch Medical Services, Incorporated at Center for Cancer Care and Research
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Montana
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Billings, Montana, United States, 59101
- CCOP - Montana Cancer Consortium
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Billings, Montana, United States, 59101
- Hematology-Oncology Centers of the Northern Rockies - Billings
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Billings, Montana, United States, 59101
- St. Vincent Healthcare Cancer Care Services
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Billings, Montana, United States, 59107-7000
- Billings Clinic - Downtown
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Bozeman, Montana, United States, 59715
- Bozeman Deaconess Cancer Center
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Butte, Montana, United States, 59701
- St. James Healthcare Cancer Care
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Great Falls, Montana, United States, 59405
- Great Falls Clinic - Main Facility
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Great Falls, Montana, United States, 59405
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Great Falls, Montana, United States, 59405-5309
- Big Sky Oncology
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Great Falls, Montana, United States, 59405
- Sletten Cancer Institute at Benefis Healthcare
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Havre, Montana, United States, 59501
- Northern Montana Hospital
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Kalispell, Montana, United States, 59901
- Kalispell Regional Medical Center
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Kalispell, Montana, United States, 59901
- Glacier Oncology, PLLC
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Kalispell, Montana, United States, 59901
- Kalispell Medical Oncology at KRMC
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Missoula, Montana, United States, 59801
- Community Medical Center
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Missoula, Montana, United States, 59807-7877
- Montana Cancer Specialists at Montana Cancer Center
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Missoula, Montana, United States, 59807
- Montana Cancer Center at St. Patrick Hospital and Health Sciences Center
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Nebraska
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Lincoln, Nebraska, United States, 68510
- Cancer Resource Center - Lincoln
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Omaha, Nebraska, United States, 68106
- CCOP - Missouri Valley Cancer Consortium
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Omaha, Nebraska, United States, 68131-2197
- Creighton University Medical Center
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North Carolina
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Rutherfordton, North Carolina, United States, 28139
- Rutherford Hospital
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North Dakota
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Bismarck, North Dakota, United States, 58501
- Bismarck Cancer Center
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Bismarck, North Dakota, United States, 58501
- Medcenter One Hospital Cancer Care Center
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Bismarck, North Dakota, United States, 58501
- Mid Dakota Clinic, PC
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Bismarck, North Dakota, United States, 58502
- St. Alexius Medical Center Cancer Center
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Fargo, North Dakota, United States, 58122
- CCOP - MeritCare Hospital
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Fargo, North Dakota, United States, 58122
- MeritCare Broadway
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Grand Forks, North Dakota, United States, 58201
- Altru Cancer Center at Altru Hospital
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Ohio
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Bellefontaine, Ohio, United States, 43311
- Mary Rutan Hospital
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Bowling Green, Ohio, United States, 43402
- Wood County Oncology Center
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Chillicothe, Ohio, United States, 45601
- Adena Regional Medical Center
-
Columbus, Ohio, United States, 43214-3998
- Riverside Methodist Hospital Cancer Care
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Columbus, Ohio, United States, 43222
- Mount Carmel Health - West Hospital
-
Columbus, Ohio, United States, 43215
- CCOP - Columbus
-
Columbus, Ohio, United States, 43215
- Grant Medical Center Cancer Care
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Columbus, Ohio, United States, 43228
- Doctors Hospital at Ohio Health
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Dayton, Ohio, United States, 45405
- Grandview Hospital
-
Dayton, Ohio, United States, 45406
- Good Samaritan Hospital
-
Dayton, Ohio, United States, 45409
- David L. Rike Cancer Center at Miami Valley Hospital
-
Dayton, Ohio, United States, 45415
- Samaritan North Cancer Care Center
-
Dayton, Ohio, United States, 45429
- CCOP - Dayton
-
Delaware, Ohio, United States, 43015
- Grady Memorial Hospital
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Elyria, Ohio, United States, 44035
- Hematology Oncology Center
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Findlay, Ohio, United States, 45840
- Blanchard Valley Medical Associates
-
Franklin, Ohio, United States, 45005-1066
- Middletown Regional Hospital
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Kettering, Ohio, United States, 45429
- Charles F. Kettering Memorial Hospital
-
Lancaster, Ohio, United States, 43130
- Fairfield Medical Center
-
Lima, Ohio, United States, 45804
- Lima Memorial Hospital
-
Marietta, Ohio, United States, 45750
- Strecker Cancer Center at Marietta Memorial Hospital
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Maumee, Ohio, United States, 43537
- Northwest Ohio Oncology Center
-
Maumee, Ohio, United States, 43537
- St. Luke's Hospital
-
Newark, Ohio, United States, 43055
- Licking Memorial Cancer Care Program at Licking Memorial Hospital
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Oregon, Ohio, United States, 43616
- St. Charles Mercy Hospital
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Oregon, Ohio, United States, 43616
- Toledo Clinic - Oregon
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Sandusky, Ohio, United States, 44870
- North Coast Cancer Care, Incorporated
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Springfield, Ohio, United States, 45505
- Community Hospital of Springfield and Clark County
-
Springfield, Ohio, United States, 45504
- Mercy Medical Center
-
Sylvania, Ohio, United States, 43560
- Flower Hospital Cancer Center
-
Tiffin, Ohio, United States, 44883
- Mercy Hospital of Tiffin
-
Toledo, Ohio, United States, 43608
- St. Vincent Mercy Medical Center
-
Toledo, Ohio, United States, 43606
- Toledo Hospital
-
Toledo, Ohio, United States, 43614
- Medical University of Ohio Cancer Center
-
Toledo, Ohio, United States, 43617
- CCOP - Toledo Community Hospital
-
Toledo, Ohio, United States, 43623
- Toledo Clinic, Incorporated - Main Clinic
-
Toledo, Ohio, United States, 43623
- St. Anne Mercy Hospital
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Troy, Ohio, United States, 45373-1300
- UVMC Cancer Care Center at Upper Valley Medical Center
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Wauseon, Ohio, United States, 43567
- Fulton County Health Center
-
Westerville, Ohio, United States, 43081
- Mount Carmel St. Ann's Cancer Center
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Wilmington, Ohio, United States, 45177
- Clinton Memorial Hospital
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Xenia, Ohio, United States, 45385
- Ruth G. McMillan Cancer Center at Greene Memorial Hospital
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Zanesville, Ohio, United States, 43701
- Genesis - Good Samaritan Hospital
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Oklahoma
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Tulsa, Oklahoma, United States, 74136
- Natalie Warren Bryant Cancer Center at St. Francis Hospital
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Pennsylvania
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Allentown, Pennsylvania, United States, 18105
- Morgan Cancer Center at Lehigh Valley Hospital - Cedar Crest
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South Carolina
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Anderson, South Carolina, United States, 29621
- AnMed Cancer Center
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Spartanburg, South Carolina, United States, 29303
- CCOP - Upstate Carolina
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Spartanburg, South Carolina, United States, 29303
- Gibbs Regional Cancer Center at Spartanburg Regional Medical Center
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South Dakota
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Rapid City, South Dakota, United States, 57701
- Rapid City Regional Hospital
-
Sioux Falls, South Dakota, United States, 57105
- Avera Cancer Institute
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Sioux Falls, South Dakota, United States, 57105
- Medical X-Ray Center, PC
-
Sioux Falls, South Dakota, United States, 57117-5039
- Sanford Cancer Center at Sanford USD Medical Center
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Virginia
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Fredericksburg, Virginia, United States, 22401
- Fredericksburg Oncology, Incorporated
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Wisconsin
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Green Bay, Wisconsin, United States, 54307-3508
- St. Vincent Hospital Regional Cancer Center
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Green Bay, Wisconsin, United States, 54301-3526
- Green Bay Oncology, Limited at St. Vincent Hospital Regional Cancer Center
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Green Bay, Wisconsin, United States, 54303
- Green Bay Oncology, Limited at St. Mary's Hospital
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Green Bay, Wisconsin, United States, 54303
- St. Mary's Hospital Medical Center - Green Bay
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Marinette, Wisconsin, United States, 54143
- Bay Area Cancer Care Center at Bay Area Medical Center
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Oconto Falls, Wisconsin, United States, 54154
- Green Bay Oncology, Limited - Oconto Falls
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Sturgeon Bay, Wisconsin, United States, 54235
- Green Bay Oncology, Limited - Sturgeon Bay
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
DISEASE CHARACTERISTICS:
- Histologically confirmed breast and/or other cancer
Undergoing first treatment with capecitabine as adjuvant (including neo-adjuvant) therapy OR for metastatic disease
- Receiving a dose of capecitabine either 2,000 mg/day (1,000 mg twice daily) OR 2,500 mg/day for 14 days with 4 courses of therapy at 3 week (+/- 3 days) intervals
- Hormone-receptor status not specified
PATIENT CHARACTERISTICS:
- Male or female
- Menopausal status not specified
- No history of allergy to urea-containing cream
- No pre-existing neuropathy ≥ grade 2
- No other dermatologic condition, that, in the opinion of the physician, may affect the hands or feet or may complicate evaluation during study treatment
PRIOR CONCURRENT THERAPY:
- No other concurrent agents that function to prevent palmar-plantar erythrodysesthesia caused by capecitabine or topical agents in the hands or feet for other indications (e.g., dryness)
- No concurrent vitamin B6 > 50 mg/day
No concurrent or planned use of over-the-counter products that contain urea or lactic acid, including any of the following:
- Aqua Care®
- Medicated Calamine^® lotion (0.3%)
- Coppertone^® Waterproof Ultra Protection Sunblock
- Dr. Scholl's^® Smooth Touch deep moisturizing cream
- Depicure^® So Smooth Cream
- Dove^® Moisturizing Cream Wash
- Cetaphil^ ®Moisturizing Cream
- Vaseline Intensive Care ^ ® lotion
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Arm I (closed to accrual as of 10/24/2007)
Patients receive topical urea/lactic acid-based cream applied to palms and soles twice daily and oral pyridoxine once daily on days 1-21.
|
Given orally
Applied topically
|
Experimental: Arm II (closed to accrual as of 10/24/2007)
Patients receive topical urea/lactic acid-based cream as in arm I (closed to accrual as of 10/24/2007) and oral placebo once daily on days 1-21.
|
Applied topically
Given orally or applied topically
|
Experimental: Arm III (closed to accrual as of 10/24/2007)
Patients receive placebo cream applied to palms and soles twice daily and pyridoxine as in arm I (closed to accrual as of 10/24/2007).
|
Given orally
Given orally or applied topically
|
Placebo Comparator: Arm IV (closed to accrual as of 10/24/2007)
Patients receive placebo cream as in arm III and oral placebo as in arm II (closed to accrual as of 10/24/2007).
|
Given orally or applied topically
|
Experimental: Arm V
Patients receive topical urea/lactic acid-based cream applied to palms and soles twice daily on days 1-21.
|
Applied topically
|
Placebo Comparator: Arm VI
Patients receive placebo cream applied to palms and soles twice daily on days 1-21.
|
Given orally or applied topically
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
To Determine Whether the Prophylactic Use of a Topical Urea/Lactic Acid Cream Can Decrease the Incidence/Severity of Capecitabine-caused Palmar-plantar Erythrodysesthesia
Time Frame: First 3 weeks of treatment
|
A patient self-reported hand-foot syndrome (HFSD), also known as palmar-plantar erythrodysesthesia, was completed daily while applying the cream.
Patients rated skin severity symptoms individually in their hands and in their feet.
Definitions of symptoms, which were based on Common Terminology Criteria for Adverse Events (CTCAE) v3.0, were provided to patients.
The number of patients reporting moderate to severe symptoms in either hands or feet were tabulated and percentages are reported.
|
First 3 weeks of treatment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
To Evaluate the Potential Toxicity of Urea/Lactic Acid Cream
Time Frame: Up to 4, 21-day cycles
|
Frequency and severity of adverse events reported by patients in weekly diary and evaluated through clinical assessment by NCI CTCAE v3.0.
The number of patients reporting grade 3 or higher events are reported in this outcome measure.
For a full list of all events, please refer to the Adverse Events section of this report.
|
Up to 4, 21-day cycles
|
Determine Whether the Prophylactic Use of Vitamin B6 Can Decrease the Incidence and/or Severity of Capecitabine-caused Palmar-plantar Erythrodysesthesia (HFSD).
Time Frame: First 3 weeks of treatment
|
A patient self-reported hand-foot syndrome diary (HFSD) was completed daily while applying the cream.
Patients rated skin severity symptoms individually in their hands and in their feet.
Definitions of symptoms, which were based on Common Terminology Criteria for Adverse Events (CTCAE) v3.0, were provided to patients.
The number of patients reporting moderate to severe symptoms were tabulated and percentages are reported.
|
First 3 weeks of treatment
|
Evaluate the Potential Toxicity of Vitamin B6.
Time Frame: up to 4, 21-day cycles
|
Frequency and severity of adverse events reported by patients in weekly diary and evaluated through clinical assessment by NCI CTCAE v3.0.
The number of patients reporting grade 3 or higher events are reported in this outcome measure.
For a full list of all events, please refer to the Adverse Events section of this report.
|
up to 4, 21-day cycles
|
Determine Whether the Prophylactic Use of a Topical Urea/Lactic Acid Cream in Combination With Vitamin B6 Can Decrease the Incidence and/or Severity of Capecitabine Caused Palmar-plantar Erythrodysesthesia.
Time Frame: First 3 weeks of treatment
|
A patient self-reported hand-foot syndrome diary (HFSD) was completed daily while applying the cream.
Patients rated skin severity symptoms individually in their hands and in their feet.
Definitions of symptoms, which were based on Common Terminology Criteria for Adverse Events (CTCAE) v3.0, were provided to patients.
The number of patients reporting moderate to severe symptoms were tabulated.
|
First 3 weeks of treatment
|
Collaborators and Investigators
Collaborators
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NCCTG-N05C5
- NCI-2009-00655 (Registry Identifier: CTRP (Clinical Trials Reporting System))
- ROCHE-NCCTG-N05C5
- CDR0000464246 (Registry Identifier: PDQ (Physician Data Query))
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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