A Study to Evaluate Efficacy and Safety of a Single Application of Capsaicin 8%Transdermal Delivery System Compared to Placebo in Reducing Pain Intensity in Subjects With Painful Diabetic Peripheral Neuropathy (PDPN) (STEP)
12 października 2015 zaktualizowane przez: Astellas Pharma Inc
A Phase III, Double-blind, Randomized, Placebo-controlled, Multicenter Study Evaluating the Efficacy and Safety of QUTENZA® in Subjects With Painful Diabetic Peripheral Neuropathy
The purpose of the study is to assess efficacy and safety of a single treatment of Capsaicin 8% transdermal delivery system in reducing pain from damaged nerves (neuropathic pain) caused by diabetes.
Przegląd badań
Status
Status
Zakończony
Warunki
Warunki
Interwencja / Leczenie
Interwencja / Leczenie
Szczegółowy opis
Participants were divided into 2 groups of approximately equal size.
In the first group, participants received a Capsaicin 8% patch applied for 30 minutes to the feet; in the second group, participants received a placebo patch applied for 30 minutes to the feet.
Participants were involved in the study for approximately 12 weeks and have visited the clinic approximately 6 times.
Typ studiów
Typ studiów
Interwencyjne
Zapisy (Rzeczywisty)
Zapisy
369
Faza
Faza
- Faza 3
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Lokalizacje studiów
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Alabama
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Anniston, Alabama, Stany Zjednoczone, 36207
- Site: 125
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California
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Fresno, California, Stany Zjednoczone, 93720
- Site: 131
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Long Beach, California, Stany Zjednoczone, 90806
- Site: 123
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Los Angeles, California, Stany Zjednoczone, 90033
- Site: 116
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Orange, California, Stany Zjednoczone, 92868
- Site: 112
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Walnut Creek, California, Stany Zjednoczone, 94597
- Site: 130
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Connecticut
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Milford, Connecticut, Stany Zjednoczone, 06460
- Site: 113
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New London, Connecticut, Stany Zjednoczone, 06320
- Site: 119
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Florida
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Boynton Beach, Florida, Stany Zjednoczone, 33435
- Site: 117
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Bradenton, Florida, Stany Zjednoczone, 34205
- Site: 124
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Clearwater, Florida, Stany Zjednoczone, 33765
- Site: 107
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Jupiter, Florida, Stany Zjednoczone, 33458
- Site: 120
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Orlando, Florida, Stany Zjednoczone, 32806
- Site: 108
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Oviedo, Florida, Stany Zjednoczone, 32765
- Site: 132
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St. Petersburg, Florida, Stany Zjednoczone, 33709
- Site: 127
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Tampa, Florida, Stany Zjednoczone, 33606
- Site: 122
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Hawaii
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Honolulu, Hawaii, Stany Zjednoczone, 96814
- Site: 133
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Massachusetts
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New Bedford, Massachusetts, Stany Zjednoczone, 02740
- Site: 126
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Michigan
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Ann Arbor, Michigan, Stany Zjednoczone, 48104
- Site: 115
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Missouri
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Hazelwood, Missouri, Stany Zjednoczone, 63042
- Site: 128
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New York
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New York, New York, Stany Zjednoczone, 10029
- Site:111
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North Carolina
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Winston-Salem, North Carolina, Stany Zjednoczone, 27103
- Site: 110
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Ohio
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Kettering, Ohio, Stany Zjednoczone, 45429
- Site: 121
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Texas
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Dallas, Texas, Stany Zjednoczone, 75230
- Site:106
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Houston, Texas, Stany Zjednoczone, 77030
- Site: 118
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Houston, Texas, Stany Zjednoczone, 77098
- Site: 114
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Lubbock, Texas, Stany Zjednoczone, 79410
- Site: 103
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San Antonio, Texas, Stany Zjednoczone, 78228
- Site: 105
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San Antonio, Texas, Stany Zjednoczone, 78229
- Site: 102
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Kryteria uczestnictwa
Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.
Kryteria kwalifikacji
Kryteria kwalifikacji
Wiek uprawniający do nauki
18 lat i starsze (Dorosły, Starszy dorosły)
Akceptuje zdrowych ochotników
Nie
Płeć kwalifikująca się do nauki
Wszystko
Opis
Inclusion Criteria:
- Diagnosis of painful, distal, symmetrical, sensorimotor polyneuropathy which is due to diabetes, for at least 1 year prior to screening visit
- Average Numeric Pain Rating Scale (NPRS) score over the last 24 hours of ≥4 at the screening and the baseline visit
Exclusion Criteria:
- Primary pain associated with PDPN (Painful Diabetic Peripheral Neuropathy) in the ankles or above
- Pain that could not be clearly differentiated from, or conditions that might interfere with the assessment of PDPN (Painful Diabetic Peripheral Neuropathy), neurological disorders unrelated to diabetic neuropathy (e.g., phantom limb pain from amputation); skin condition in the area of the neuropathy that could alter sensation (e.g., plantar ulcer)
- Current or previous foot ulcer as determined by medical history and medical examination
- Any amputation of lower extremity
- Severe renal disease as defined by a creatinine clearance of <30 ml/min calculated according to the Cockcroft-Gault formula
- Clinically significant cardiovascular disease within 6 months prior to screening visit defined as cerebrovascular accident, unstable or poorly controlled hypertension, transient ischemic attack, myocardial infarction, unstable angina, current arrhythmia, any heart surgery including coronary artery bypass graft surgery, percutaneous coronary angioplasty/stent placement, or valvular heart disease
- Significant peripheral vascular disease (intermittent claudication or lack of pulsation of either the dorsalis pedis or posterior tibial artery, or ankle-brachial systolic blood pressure index of <0.80)
- Clinically significant foot deformities, including hallux rigidus, hallux valgus, or rigid toe as determined by physical examination as judged by the investigator
- Clinically significant ongoing, uncontrolled or untreated abnormalities in cardiac, renal, hepatic, or pulmonary function that may interfere either with the ability to complete the study or the evaluation of adverse events
- Diagnosis of any poorly controlled major psychiatric disorder
- Active substance abuse or history of chronic substance abuse within 1 year prior to screening visit or any prior chronic substance abuse (including alcoholism) likely to re-occur during the study period as judged by the investigator
- Hypersensitivity to capsaicin (i.e., chili peppers or over-the-counter [OTC] capsaicin products), any Capsaicin 8% transdermal delivery system excipients, Eutectic Mixture of Local Anaesthetics (EMLA) ingredients or adhesives
- Use of any topical pain medication, such as non-steroidal anti-inflammatory drugs, menthol, methyl salicylate, local anesthetics, steroids or capsaicin products on the painful areas within 7 days preceding the first patch application at the baseline visit
- Use of oral or transdermal opioids exceeding a total daily dose of morphine of 80 mg/day, or equivalent; or any parenteral opioids, regardless of dose, within 7 days preceding the first patch application at the baseline visit
- Skin areas to be treated with Capsaicin 8% transdermal delivery system showing changes such as crusting or ulcers
- Planned elective surgery during the trial
Plan studiów
Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Poczwórny
Liczba ramion
2
Broń i interwencje
Grupa uczestników / ArmGrupa uczestników / Arm |
Interwencja / LeczenieInterwencja / Leczenie |
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Eksperymentalny: Capsaicin 8%
Capsaicin 8% patch was applied for 30 minutes to the painful area(s) on Day 1
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Capsaicin 8% transdermal delivery system
Inne nazwy:
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Komparator placebo: Placebo
Placebo patch was applied for 30 minutes to the painful area(s) on Day 1
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Placebo Patch
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Co mierzy badanie?
Podstawowe miary wyniku
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Percent Change in the Average Daily Pain Score From Baseline to Between Weeks 2 and 8
Ramy czasowe: Baseline to between Weeks 2 to 8
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Percent change in the average daily pain score from baseline to between Weeks 2 and 8, measured using Question 5 of the Brief Pain Inventory-Diabetic Neuropathy (BPI-DN).
Participants assessed their pain due to diabetes in the last 24 hours on a numeric rating scale from 0 (no pain) to 10 (pain as bad as you can imagine).
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Baseline to between Weeks 2 to 8
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Miary wyników drugorzędnych
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Percent Change in the Average Daily Pain Score From Baseline to Between Weeks 2 and 12
Ramy czasowe: Baseline to between Weeks 2 and 12
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Percent Change in the Average Daily Pain Score from baseline to between Weeks 2 and 12 measured using Question 5 of the Brief Pain Inventory-Diabetic Neuropathy (BPI-DN).
Participants assessed their pain due to diabetes in the last 24 hours on a numeric rating scale from 0 (no pain) to 10 (pain as bad as you can imagine).
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Baseline to between Weeks 2 and 12
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Weekly Percent Change From Baseline in Average Daily Pain Score
Ramy czasowe: Baseline to Weeks 2, 3, 4, 5, 6, 7, 8, 9,10, 11 and 12
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Weekly Percent Change from baseline in average daily pain score from baseline to Week 12 measured using Question 5 of the Brief Pain Inventory-Diabetic Neuropathy (BPI-DN).
Participants assessed their pain due to diabetes in the last 24 hours on a numeric rating scale from 0 (no pain) to 10 (pain as bad as you can imagine).
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Baseline to Weeks 2, 3, 4, 5, 6, 7, 8, 9,10, 11 and 12
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Weekly Average of Average Daily Pain at Baseline and Every Week After Baseline
Ramy czasowe: Baseline and Weeks 2, 4, 8 and 12
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Weekly average of average daily pain score at Baseline and Weeks 2,4,8 and 12 measured using Question 5 of the Brief Pain Inventory-Diabetic Neuropathy (BPI-DN).
Participants assessed their pain due to diabetes in the last 24 hours on a numeric rating scale from 0 (no pain) to 10 (pain as bad as you can imagine).
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Baseline and Weeks 2, 4, 8 and 12
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Percentage of Participants With 30% Reduction in Average Daily Pain Score.
Ramy czasowe: Baseline, Weeks 2-8 and Weeks 2-12
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Percentage of participants achieving 30% decrease in the average daily pain score in Weeks 2 and 8 and Weeks 2 and 12 measured using Question 5 of the Brief Pain Inventory-Diabetic Neuropathy (BPI-DN).
Participants assessed their pain on a numeric rating scale from 0 (no pain) to 10 (pain as bad as you can imagine).
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Baseline, Weeks 2-8 and Weeks 2-12
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Percentage of Participants With 50% Reduction in Average Daily Pain Score.
Ramy czasowe: Baseline, Weeks 2-8 and Weeks 2-12
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Percentage of participants achieving 50% decrease in the average daily pain score in Weeks 2 and 8 and Weeks 2 and 12 measured using Question 5 of the Brief Pain Inventory-Diabetic Neuropathy (BPI-DN).
Participants assessed their pain on a numeric rating scale from 0 (no pain) to 10 (pain as bad as you can imagine).
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Baseline, Weeks 2-8 and Weeks 2-12
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Overall Participant Status Assessed Using Patient Global Impression of Change (PGIC) Self-assessment Questionnaire in Week 2
Ramy czasowe: Baseline to Week 2
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Overall participant status assessed using Patient Global Impression of Change (PGIC) self-assessment questionnaire which was used by participants to report on 7 categories listed as follows; Very Much Improved, Much Improved, Minimally Improved, No Change, Minimally Worse, Much Worse and Very Much Worse in Week 2
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Baseline to Week 2
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Overall Participant Status Assessed Using Patient Global Impression of Change (PGIC) Self-assessment Questionnaire in Week 8
Ramy czasowe: Baseline to Week 8
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Overall participant status assessed using Patient Global Impression of Change (PGIC) self-assessment questionnaire which was used by participants to report on 7 categories listed as follows; Very Much Improved, Much Improved, Minimally Improved, No Change, Minimally Worse, Much Worse and Very Much Worse in Week 8
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Baseline to Week 8
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Overall Participant Status Assessed Using Patient Global Impression of Change (PGIC) Self-assessment Questionnaire in Week 12
Ramy czasowe: Baseline to Week 12
|
Overall participant status assessed using Patient Global Impression of Change (PGIC) self-assessment questionnaire which was used by participants to report on 7 categories listed as follows; Very Much Improved, Much Improved, Minimally Improved, No Change, Minimally Worse, Much Worse and Very Much Worse in Week 12
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Baseline to Week 12
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Change From Baseline in the European Quality Of Life (QOL) Questionnaire in 5 Dimensions (EQ-5D) With Visual Analog Scale (VAS) to Weeks 2, 8 and 12
Ramy czasowe: Baseline to Weeks 2, 8 and 12
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Change from Baseline in the European Quality Of Life (QOL) questionnaire in 5 dimensions (EQ-5D) with Visual Analog Scale (VAS) to Weeks 2, 8 and 12. EQ-5D self-reported questionnaire is used to measure health-related quality of life by measuring 5 dimensions of health: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression.
The EQ-5D questionnaire includes a visual analog scale (VAS) which records participants self-rated health status on a graduated (0-100) scale with higher scores indicating higher Health-Related Quality of Life (HRQoL).
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Baseline to Weeks 2, 8 and 12
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Change in Hospital Anxiety and Depression Scale (HADS) Anxiety Scale From Baseline to Weeks 2, 8 and 12
Ramy czasowe: Baseline to Weeks 2, 8 and 12
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The Hospital Anxiety and Depression Scale (HADS) is a self-report scale developed for the assessment of anxiety and depression, that contain 14 items rated on a 4-point Likert-type scale.
There are 2 subscales,one assessing depression and the other anxiety.
The 7-item depression and anxiety subscales yield scores of 0 to 21 that are interpreted with the following cut-off points: 0 to 7, normal; 8 to 10, mild mood disturbance; 11 to 14, moderate mood disturbance; and 15 to 21, severe mood disturbance.
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Baseline to Weeks 2, 8 and 12
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Change in Hospital Anxiety and Depression Scale (HADS) Depression Scale From Baseline to Weeks 2, 8 and 12.
Ramy czasowe: Baseline to Weeks 2, 8 and 12
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The Hospital Anxiety and Depression Scale (HADS) is a self-report scale developed for the assessment of anxiety and depression, it contains 14 items rated on a 4-point Likert-type scale.
There are 2 subscales,one assessing depression and the other anxiety.
The 7-item depression and anxiety subscales yield scores of 0 to 21 that are interpreted with the following cut-off points: 0 to 7, normal; 8 to 10, mild mood disturbance; 11 to 14, moderate mood disturbance; and 15 to 21, severe mood disturbance.
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Baseline to Weeks 2, 8 and 12
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Treatment Satisfaction Assessment Based on Self-Assessment of Treatment (SAT II) Questionnaire at Baseline, Weeks 8 and 12
Ramy czasowe: Baseline, Weeks 8 and 12
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Treatment satisfaction assessment based on Self-Assessment Treatment (SAT II) questionnaire and the question "Over the past 7 days, how much has the study treatment improved your pain level?"
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Baseline, Weeks 8 and 12
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Percent Change in Average Sleep Interference Score From Baseline to Between Weeks 2-8 and Weeks 2-12
Ramy czasowe: Baseline, Weeks 2-8 and Weeks 2-12
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Percent change in average sleep interference was measured by Question 9F of the Brief Pain Inventory-Diabetic Neuropathy (BPI DN) and was used to assess pain and sleep interference index.
Daily sleep interference rating scale consists of an 11-point numerical scale with which the patient describes how pain related to diabetes has interfered with their sleep during the past 24 hours.
On a scale 0 identifies "pain does not interfere with sleep" and 10 identifies "pain completely interferes with sleep".
Average sleep interference score is assessed from baseline to Weeks 2-8 and Weeks 2-12.
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Baseline, Weeks 2-8 and Weeks 2-12
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Tolerability of Patch Application Assessed by Dermal Assessment on Day 1, 15 Minutes and 60 Minutes After Patch Removal.
Ramy czasowe: Day 1, 15 minutes and 60 minutes after patch removal
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Tolerability of patch application was assessed by dermal assessment (0 to 7 point severity score on Dermal Assessment Scale).
Data reported is based on the number of participants in the combined category with a score ≥ 4 (Definite edema or higher), 15 and 60 minutes after patch removal.
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Day 1, 15 minutes and 60 minutes after patch removal
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Change From Pre-application in"Pain Now" Score
Ramy czasowe: Pre-application and 15 minutes and 60 minutes after patch removal
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Change from pre-application in"Pain Now" score was measured on a scale from 0-10 where 0 equates to "No Pain" and 10 to "Pain as bad as you can imagine".
Participants were asked to provide pain ratings relative only to the area of pain undergoing treatment.
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Pre-application and 15 minutes and 60 minutes after patch removal
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Number of Participants Who Used Rescue Pain Medication Days 1 Through 5
Ramy czasowe: Days 1 - 5
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Summarized number of participants who used Rescue Pain Medications for Pain
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Days 1 - 5
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Safety Assessed Through Adverse Events (AE) and Serious Adverse Events (SAE), Vital Signs, and Laboratory Analyses From Baseline to Week 12
Ramy czasowe: Baseline to Week 12
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Number of patients assessed for Safety through Adverse Events (AE) and Serious Adverse Events (SAE), vital signs, and laboratory analyses from baseline to week 12
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Baseline to Week 12
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Współpracownicy i badacze
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Sponsor
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Publikacje i pomocne linki
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Przydatne linki
Daty zapisu na studia
Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.
Główne daty studiów
Rozpoczęcie studiów
Rozpoczęcie studiów
1 lutego 2012
Zakończenie podstawowe (Rzeczywisty)
Zakończenie podstawowe
1 lutego 2014
Ukończenie studiów (Rzeczywisty)
Ukończenie studiów
1 lutego 2014
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany
12 lutego 2012
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy przesłany, który spełnia kryteria kontroli jakości
14 lutego 2012
Pierwszy wysłany (Oszacować)
Pierwszy wysłany
15 lutego 2012
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Oszacować)
Ostatnia wysłana aktualizacja
4 listopada 2015
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
12 października 2015
Ostatnia weryfikacja
Ostatnia weryfikacja
1 października 2015
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
- Choroby Układu Nerwowego
- Choroby układu hormonalnego
- Powikłania cukrzycy
- Cukrzyca
- Choroby nerwowo-mięśniowe
- Choroby obwodowego układu nerwowego
- Neuropatie cukrzycowe
- Fizjologiczne skutki leków
- Agenty obwodowego układu nerwowego
- Agenci systemu sensorycznego
- Środki dermatologiczne
- Przeciwświądowe
- Kapsaicyna
Inne numery identyfikacyjne badania
Inne numery identyfikacyjne badania
- E05-CL-3004
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .