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Anti-metabolites

Treatment arm for Arterial Restenosis

N/A
Waitlist Available
Led By Kong Teng Tan, MD
Research Sponsored by University Health Network, Toronto
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 12 months post index procedure
Awards & highlights

Study Summary

The purpose of the study is to evaluate the safety and efficacy on the use of drug eluting balloon (DEB) with paclitaxel to treat in-stent restenosis in femoropopliteal arteries.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months post index procedure
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 months post index procedure for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Target lesion patency at 6-month follow-up.
Secondary outcome measures
Clinical success up to 12 months post index procedure

Trial Design

1Treatment groups
Active Control
Group I: Treatment armActive Control1 Intervention
SFA angioplasty with In.Pact Admiral drug eluting balloon

Find a Location

Who is running the clinical trial?

University Health Network, TorontoLead Sponsor
1,472 Previous Clinical Trials
484,963 Total Patients Enrolled
Kong Teng Tan, MDPrincipal InvestigatorUniversity Health Network, Toronto
3 Previous Clinical Trials
50 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Paclitaxel Eluting Balloon for SFA In-stent Restenosis
2012. "Paclitaxel Eluting Balloon for SFA In-stent Restenosis". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT01616888.
All > Acl
~2 spots leftby Apr 2025
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