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NCT03041467 · ClinicalTrials.gov registry record · NA
IN.PACT™ AV Access IDE Study
A NA study, sponsored by Medtronic Endovascular.
- Completed
- Registry status
- NA
- Development phase
- 330
- Enrollment target
NCT03041467: Completed NA study, sponsored by Medtronic Endovascular.
NCT03041467 is a NA study that has completed, run by Medtronic Endovascular. The registered enrollment target is 330 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (76% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03041467, a NA study, has completed, sponsored by Medtronic Endovascular.
- COMPLETED
- Registry status
- NA
- Development phase
- 330 participants
- Enrollment target
Study Summary
To evaluate the safety and efficacy of the IN.PACT™ AV Access Drug Coated Balloon (DCB) compared to percutaneous transluminal angioplasty (PTA) for treatment of subjects presenting with de novo or non-stented restenotic obstructive lesion of native arteriovenous dialysis fistulae (AVF) in the upper extremity.
Primary Outcome
Freedom from clinically-driven target lesion revascularization (CD-TLR) or access circuit thrombosis measured through 6 months post-procedure.
Interventions
- DEVICE IN.PACT AV DCB
- DEVICE Standard Balloon Angioplasty
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 330 participants |
| Start Date | 2017-04-25 |
| Est. Completion | 2023-05-05 |
| Phase | NA |
What the finished NCT03041467 record still lists
NCT03041467 is an interventional study that assigns participants to a tested intervention. The registered 330 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (76% lower).
The record links to 0 conditions, and to 2 interventions - of which IN.PACT AV DCB is the first listed.
NCT03041467 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03041467 about?
NCT03041467 is a clinical study titled "IN.PACT™ AV Access IDE Study". To evaluate the safety and efficacy of the IN.PACT™ AV Access Drug Coated Balloon (DCB) compared to percutaneous transluminal angioplasty (PTA) for treatment of subjects presenting with de novo or non-stented restenotic obstructive lesion of native arteriovenous dialysis fistulae (AVF) in the upper ...
What is the current status of trial NCT03041467?
This trial is currently completed. It is a NA study. The enrollment target is 330 participants. The study started on 2017-04-25. Estimated completion is 2023-05-05.
What interventions are being tested in trial NCT03041467?
The interventions under investigation include: IN.PACT AV DCB (DEVICE), Standard Balloon Angioplasty (DEVICE).
Who is sponsoring clinical trial NCT03041467?
This trial is sponsored by Medtronic Endovascular, which has 25 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03041467's enrollment target sits among peer trials
330 307th of 2000 higher than 1,693 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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