Prevention of Restenosis Following Revascularization
A Phase II Trial of ABI-007 (Paclitaxel Albumin-bound Particles) for the Prevention of Restenosis Following Revascularization of the Superficial Femoral Artery (SFA)
Tutkimuksen yleiskatsaus
Tila
Tila
Ehdot
Ehdot
Interventio / Hoito
Interventio / Hoito
Opintotyyppi
Opintotyyppi
Ilmoittautuminen (Todellinen)
Ilmoittautuminen
Vaihe
Vaihe
- Vaihe 2
Yhteystiedot ja paikat
Opiskelupaikat
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California
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Sacramento, California, Yhdysvallat, 95817
- UC Davis Medical Center, Ellison Ambulatory Care Center Cardiology Suite 3400
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Florida
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Gainsville, Florida, Yhdysvallat, 32605
- Vascular & Interventional Physicians
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Iowa
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Davenport, Iowa, Yhdysvallat, 52803
- Midwest Cardiovascular Research Foundation
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Michigan
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Flint, Michigan, Yhdysvallat, 48507
- Michigan Vascular Research Center
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New Jersey
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Teaneck, New Jersey, Yhdysvallat, 07666
- Holy Name Hospital
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Ohio
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Cincinnati, Ohio, Yhdysvallat, 45219
- Lindner Clinical Trials Center
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Rhode Island
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Providence, Rhode Island, Yhdysvallat, 02903
- Rhode Island Hospital
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Osallistumiskriteerit
Kelpoisuusvaatimukset
Kelpoisuusvaatimukset
Opintokelpoiset iät
Hyväksyy terveitä vapaaehtoisia
Sukupuolet, jotka voivat opiskella
Kuvaus
Inclusion Criteria:
- Male or non-pregnant and non-lactating female and greater than or equal to 18 years of age. All females if child bearing potential must have a negative serum pregnancy test
- Patient is determined to have peripheral artery disease (PAD) classified as Rutherford category 1-4 (grade I/II) - mild, moderate, or severe claudication or ischemic rest pain
- Patient has de novo lesion causing occlusion or an angiographic stenosis of at least 50% in the superficial femoral artery
- Patient has a single or multiple lesions located in the superficial femoral artery with a total length 5-15 cm.
- Normal vessel diameter of the SFA is 4-6 mm
- Patient must have a visibly patent (by angiography) popliteal artery below the target lesion
- No residual flow limiting dissection or residual stenosis greater 30% (visual estimate) after percutaneous balloon angioplasty (PTA) or provisional stenting. Treatment with provisional stenting will be allowed only for flow-limiting dissection, grade C/D or greater than 30 % residual stenosis angiographically after angioplasty alone.
- No target vessel thrombosis confirmed angiography post-PTA procedure
- No distal embolization within target limb
- Patient or his/her legally authorized representative or guardian has been informed about the nature of the study, and has agreed to participate in the study, and signed the Informed Consent Form prior to any premedication, prior to performance of revascularization procedures, and prior to participation in any study-related activities
Exclusion Criteria:
- Women of child bearing potential who do not use adequate contraception
- Patients who have experienced acute onset of claudication
- History of bleeding diathesis, coagulopathy, platelet disorder, or thrombocytopenia
- Patients with lesions requiring treatment with atherectomy or primary stenting
- Target lesion in which PTA failure would require treatment by provisional stenting with more than 2 stents
- Patient has a life expectancy of less than 36 months or there are factors making clinical follow up difficult (no fixed address, etc)
- Additional planned vascular procedure in treated extremity (note that concurrent endovascular treatment of iliac disease is allowable)
- Patient is immunosuppressed or is HIV positive
- Any individual who may refuse a blood transfusion
- Documented major gastrointestinal bleeding within 3 months
- The following lab values at baseline are exclusionary:
- Serum creatinine greater or equal to 2.5 mg/dl
- Platelet count less than 100,000 cells/mm^3
- Uncorrectable coagulopathy with international normalized ratio (INR) greater than 2.0
- Absolute Neutrophil Count (ANC) less than 2000 cells mm^3
- Hemoglobin (Hgb) less than 9 g/dl
- Total Bilirubin greater than 1.5 mg/dl
- Alanine transaminase (SGPT) greater than 2.5 x upper limit normal range (ULN)
- Aspartate transaminase (SGOT) greater than 2.5 x ULN
- Alkaline phosphatase greater than 2.5 x ULN
- Total cholesterol greater than 350 mg/dl or Low Density Lipoprotein greater than 200 mg/dl
- Known allergies/hypersensitivity/contraindication to the study drug, to taxanes, to any required study treatment:aspirin, heparin, clopidogrel bisulfate, stent materials, or to ticlopidine, or dipyridamole
- Patient treated with bivalirudin (Angiomax)
- Pre-existing sensory neuropathy of National Cancer Institute (NCI) Toxicity Grade >1
- Previous participation in another study with any investigational drug or device within the past 30 days or current enrollment in any other clinical protocol or investigational trial
- Renal failure requiring hemodialysis
- Lower extremity or pedal pulse
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Ennaltaehkäisy
- Jako: Satunnaistettu
- Inventiomalli: Rinnakkaistehtävä
- Naamiointi: Ei mitään (avoin tarra)
Aseiden lukumäärä
Aseet ja interventiot
Osallistujaryhmä / ArmOsallistujaryhmä / Arm |
Interventio / HoitoInterventio / Hoito |
|---|---|
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Ei väliintuloa: No Drug Treatment Control
Following revascularization, participants did not receive any study drug treatment.
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Kokeellinen: Proximal to Lesion + IV
Participants received an initial intraarterial infusion (proximal to the lesion) of 45 mg/m^2 nanoparticle paclitaxel immediately following revascularization, and a follow-up intravenous injection of 45 mg/m^2 at 7 days.
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Nanoparticle albumin-bound paclitaxel, 45 mg/m^2.
Muut nimet:
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Kokeellinen: During Flow Arrest
Participants received an initial intraarterial infusion (during flow arrest) of 45 mg/m^2 nanoparticle paclitaxel immediately following revascularization.
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Nanoparticle albumin-bound paclitaxel, 45 mg/m^2.
Muut nimet:
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Kokeellinen: During Flow Arrest + IV
Participants received an initial intraarterial infusion (during flow arrest) of 45mg/m^2 nanoparticle paclitaxel immediately following revascularization and a follow-up intravenous injection of 45 mg/m^2 at 7 days.
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Nanoparticle albumin-bound paclitaxel, 45 mg/m^2.
Muut nimet:
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Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Target Vessel Revascularization at 9 Months
Aikaikkuna: 9 months
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Target vessel revascularization (TVR) was defined as percutaneous revascularization or bypass of the target lesion or any segment of the artery containing the target lesion.
The percentage of participants requiring revascularization of the target vessel was determined by stenosis of > 50% confirmed by angiography.
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9 months
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Toissijaiset tulostoimenpiteet
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Systolic Velocity Ratio (SVR) > 2.0
Aikaikkuna: 9 months
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The percentage of participants with a systolic velocity ratio > 2.0 assessed using lower extremity arterial duplex ultrasound.
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9 months
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Change From Baseline in Walking Impairment Questionnaire (WIQ) Score
Aikaikkuna: Baseline and Month 9
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The Walking Impairment Questionnaire (WIQ) is utilized to characterize a patient's walking ability.
Scores range from 0 (no difficulty) to 100 (much difficulty).
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Baseline and Month 9
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Decrease in Ankle Brachial Index (ABI) > 0.15
Aikaikkuna: Baseline and Month 9
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The percentage of participants with a decrease in the Ankle Brachial Index (ABI) > 0.15. Ankle Brachial Index = Systolic Ankle Pressure / Systolic Brachial Pressure. |
Baseline and Month 9
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Target Lesion Revascularization (TLR) at 9 Months
Aikaikkuna: 9 months
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Target lesion revascularization (TLR) was defined as repeat percutaneous intervention or bypass surgery of the previously treated target lesion (or blockage).
The percentage of participants requiring revascularization of the target lesion was determined by stenosis of > 50% confirmed by angiography.
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9 months
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Number of Deaths
Aikaikkuna: Up to 11 months
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Number of patients who died due to any cause.
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Up to 11 months
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Number of Participants With Myocardial Infarction (MI)
Aikaikkuna: Up to 11 months
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The number of patients experiencing Myocardial Infarction (MI) during the study.
Myocardial Infarction was defined as new pathologic Q waves of at least 0.04 seconds, or an increase in serum creatine kinase to more than twice the normal code together with a pathologic increase in myocardial isoenzymes.
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Up to 11 months
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Number of Participants With a Stroke
Aikaikkuna: Up to 11 months
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The number of patients experiencing a stroke during the study.
Stroke was defined as any sudden development of neurological deficits lasting more than 24 hours, and if a brain imaging study is performed it shows an infarction or hemorrhage.
A transient ischemic attack is a neurological deficit lasting less than 24 hours and, if an imaging study is performed, shows no evidence of infarction or hemorrhage.
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Up to 11 months
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Minimum Lumen Diameter
Aikaikkuna: 9 months
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Minimum lumen diameter (MLD) is defined as the smallest diameter in millimeters (mm) in the arterial segment of interest measured angiographically.
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9 months
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Late Loss
Aikaikkuna: Day 1 (following revascularization) and 9 months
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Late loss is defined as minimum lumen diameter (MLD) immediately post-procedure minus MLD at the time of follow-up, in mm.
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Day 1 (following revascularization) and 9 months
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Percentage of Participants With Binary Restenosis
Aikaikkuna: 9 months
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Binary restenosis was defined by a >50% diameter stenosis at follow-up study, assessed by angiography.
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9 months
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Diameter Stenosis
Aikaikkuna: 9 months
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Diameter stenosis is calculated as [1 - (minimum lumen diameter (MLD) / reference vessel diameter)] * 100, where the reference vessel diameter is the vessel diameter measured in a healthy segment of the target vessel proximal as close as possible to the lesion.
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9 months
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Yhteistyökumppanit ja tutkijat
Sponsori
Sponsori
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus
Opiskelun aloitus
Ensisijainen valmistuminen (Todellinen)
Ensisijainen valmistuminen
Opintojen valmistuminen (Todellinen)
Opintojen valmistuminen
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Arvio)
Ensimmäinen Lähetetty
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Arvio)
Viimeisin päivitys julkaistu
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Avainsanat
Muita asiaankuuluvia MeSH-ehtoja
- Sydän-ja verisuonitaudit
- Valtimotauti
- Valtimon tukossairaudet
- Ateroskleroosi
- Verisuonisairaudet
- Ääreisvaltimotauti
- Perifeeriset verisuonisairaudet
- Farmakologisen vaikutuksen molekyylimekanismit
- Antineoplastiset aineet
- Tubuliinimodulaattorit
- Antimitoottiset aineet
- Mitoosin modulaattorit
- Antineoplastiset aineet, fytogeeniset
- Paklitakseli
- Albumiiniin sitoutunut paklitakseli
Muut tutkimustunnusnumerot
Muut tutkimustunnusnumerot
- CVR002
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