# IN.PACT™ AV Access Post-Approval Study (PAS002)

> **NCT04543539** · — · ACTIVE_NOT_RECRUITING · sponsor: **Medtronic** · enrollment: 240 (actual)

## Conditions studied

- Arteriovenous Fistula
- Arteriovenous Fistula Stenosis
- Arteriovenous Fistula Occlusion
- Fistula

## Interventions

- **COMBINATION_PRODUCT:** IN.PACT™ AV Drug Coated Balloon (DCB) - Primary Cohort
- **COMBINATION_PRODUCT:** IN.PACT™ AV Drug Coated Balloon (DCB) - Extended Cohort

## Key facts

- **NCT ID:** NCT04543539
- **Lead sponsor:** Medtronic
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** ACTIVE_NOT_RECRUITING
- **Start date:** 2020-11-13
- **Primary completion:** 2025-06-03
- **Final completion:** 2029-02
- **Target enrollment:** 240 (ACTUAL)
- **Last updated:** 2025-10-20


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04543539

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04543539, "IN.PACT™ AV Access Post-Approval Study (PAS002)". Retrieved via AI Analytics 2026-09-28 from https://api.ai-analytics.org/clinical/NCT04543539. Licensed CC0.

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