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WRAP North America

StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

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  1. Minor Study sites revised (16)v7
  2. Minor Trial sites expanded: 12 → 16 locationsv6
  3. Minor Study sites: 4 to 12v5
  4. Minor Study sites: 3 to 4
    • Secondary endpoints: details revised at 1 of 4 entries
    v4
  5. Minor Re-verified, no change to tracked fieldsv3
  6. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 3
    • Start date changed from estimate of Jun 2025 to Jul 31, 2025
    v2
  7. Minor 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
The goal of this observational study is to investigate the safety and efficacy of the WRAPSODY CIE in a real-world North American population. Participants treated with the WRAPSODY CIE device in accordance with the device instructions for use will be followed in accordance with standard of care up to 3-years post-procedure.
Trial Details
NCT Number NCT06807099
Lead Sponsor Merit Medical Systems, Inc.
Conditions
(from sponsor)
Venous Stenosis, Venous Occlusion
Related terms Arteriovenous Fistula
Enrollment 250 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov