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Anti-mitotic Agent
Paclitaxel for Peripheral Arterial Disease (PacTAP Trial)
N/A
Waitlist Available
Led By Eric J Dippel, MD
Research Sponsored by Midwest Cardiovascular Research Foundation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 and 12 months
Awards & highlights
PacTAP Trial Summary
The purpose of this study is to assess the safety and efficacy of administering intra-arterial paclitaxel in the femoropopliteal arteries via the TAPAS catheter following percutaneous revascularization to prevent restenosis.
Eligible Conditions
- Peripheral Arterial Disease
- Restenosis
PacTAP Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 and 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 and 12 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Primary Patency
Primary Safety
Secondary outcome measures
Functional Status
Primary Assisted Patency
Primary Patency at 12 months
+2 morePacTAP Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: PaclitaxelActive Control1 Intervention
Group II: PlaceboPlacebo Group1 Intervention
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Who is running the clinical trial?
Midwest Cardiovascular Research FoundationLead Sponsor
5 Previous Clinical Trials
224 Total Patients Enrolled
3 Trials studying Peripheral Arterial Disease
136 Patients Enrolled for Peripheral Arterial Disease
Spectranetics CorporationIndustry Sponsor
25 Previous Clinical Trials
4,342 Total Patients Enrolled
15 Trials studying Peripheral Arterial Disease
4,055 Patients Enrolled for Peripheral Arterial Disease
Eric J Dippel, MDPrincipal InvestigatorMidwest Cardiovascular Research Foundation
1 Previous Clinical Trials
252 Total Patients Enrolled
1 Trials studying Peripheral Arterial Disease
252 Patients Enrolled for Peripheral Arterial Disease
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