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BIOTRONIK Dynetic-35 Stent for the Treatment of Peripheral Iliac Lesions

Study acronym: BIONETIC-I
StatusActive, Not Recruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

  1. Trial status: Recruiting to Active, Not Recruiting Enrollment target: estimated 159 to confirmed 160 · Study sites: 13 to 15 · Primary completion date changed from estimate of Sep 2023 to Feb 28, 2023 · 2 morev4 Show 5 more changesShow less
    • Enrollment target: estimated 159 to confirmed 160
    • Study sites: 13 to 15
    • Primary completion date changed from estimate of Sep 2023 to Feb 28, 2023
    • Completion date: Sep 2027 to Feb 28, 2028
    • Eligibility criteria expanded, about 7 words

    See this version in full on ClinicalTrials.gov ↗

  2. Study sites: 2 to 13v3
  3. Trial status: Not Yet Recruiting to Recruiting Study sites: 0 to 2 · Start date changed from estimate of Sep 2021 to Aug 10, 2021v2 Show 2 more changesShow less
    • Study sites: 0 to 2
    • Start date changed from estimate of Sep 2021 to Aug 10, 2021
  4. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
BIOTRONIK cobalt chromium balloon-expandable Dynetic-35 stent in association with Passeo-35 Xeo peripheral dilation catheter for the treatment of peripheral iliac lesions
Trial Details
NCT Number NCT04830228
Lead Sponsor Biotronik AG
Conditions Peripheral Artery Disease
Enrollment 160 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov