Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT06710795 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

AFFIX: Post-market Study of MaxTack™ Motorized Fixation Device in Subjects Undergoing Ventral Hernia Repair

Study acronym: AFFIX
StatusActive, Not Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 4 months later Mar 23, 2026 → Jul 28, 2026
See other at-risk trials from Medtronic - MITG

Record History

See every version on ClinicalTrials.gov ↗

  1. Primary completion pushed from Mar 23, 2026 to Jul 28, 2026v5
  2. Enrollment reduced: 110 → 35 participantsv4 Show 5 more changesShow less
    • Start date: Nov 26, 2024 to Jun 16, 2025
    • Trial status changed: Recruiting → Active, Not Recruiting
    • Study completion pushed from Feb 15, 2027 to May 7, 2027
    • Primary completion date changed from estimate of Mar 15, 2026 to Mar 23, 2026
    • Site details revised at 3 of 3 sites
  3. Site contacts updated at 1 of 3 sitesv3
  4. Primary endpoints: 1 to 2
    • Study sites: 1 to 3
    • Secondary endpoints: details revised at 2 of 10 entries
    • Study description expanded, about 39 words
    v2
  5. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 is sponsoring and funding the AFFIX study, a prospective, post-market, multicenter, nonrandomized, single-arm, interventional clinical study. The purpose of this study is to evaluate the performance and safety of the MaxTack™ Motorized Fixation Device when used for fixation of prosthetic material to soft tissue in minimally invasive ventral hernia repair procedures.
Trial Details
NCT Number NCT06710795
Lead Sponsor Medtronic - MITG
Conditions
(from sponsor)		 Ventral Hernia
Related terms Hernia, Ventral
Enrollment 35 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov