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

StatusActive, Not Recruiting
PhaseNot specified
SponsorMedtronic
Started
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Record History

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  1. Primary completion date changed from estimate of Jun 2025 to Jun 3, 2025v20
  2. Primary completion date: Feb 2025 to Jun 2025v19
  3. Re-verified, no change to tracked fieldsv18
  4. Trial status: Recruiting to Active, Not Recruiting
    • Site details revised at 20 of 20 sites
    v17
  5. Study sites: 19 to 20v16
Show 14 earlier versionsHide 14 earlier versions
  1. Study sites: 18 to 19v15
  2. Study sites: 17 to 18v14
  3. Study sites: 16 to 17
    • Eligibility criteria expanded, about 12 words
    v13
  4. Study sites: 13 to 16v12
  5. Site details revised at 1 of 13 sitesv11
  6. Study sites: 12 to 13
    • Primary completion date: Oct 2025 to Feb 2025
    • Study completion date: Oct 2027 to Feb 2029
    v10
  7. Study sites: 10 to 12v9
  8. Study sites: 8 to 10v8
  9. Study sites: 6 to 8v7
  10. Study sites: 4 to 6v6
  11. Study sites: 2 to 4v5
  12. Study sites: 1 to 2v4
  13. Eligibility criteria expanded, about 39 wordsv3
  14. Trial status: Not Yet Recruiting to Recruitingv2 Show 4 more changesShow less
    • Study sites: 0 to 1
    • Primary completion date: Oct 17, 2025 to Oct 2025
    • Study completion date: Oct 17, 2027 to Oct 2027
    • Start date changed from estimate of Oct 17, 2020 to Nov 13, 2020
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Medtronic
16 trials monitored
See all monitored trials
Long-term safety will be summarized
Trial Details
NCT Number NCT04543539
Lead Sponsor Medtronic
Conditions
(from sponsor)		 Arteriovenous Fistula, Arteriovenous Fistula Stenosis, Arteriovenous Fistula Occlusion, Fistula
Related terms Arteriovenous Fistula, Fistula
Enrollment 240 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov