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

Running, not enrolling · Not applicable

Conditions studied: Ventral Hernia

In brief

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.

Key facts

Study ID

NCT06710795

Run by

Medtronic - MITG

People needed

35

Starts

2025-06-16

Expected to finish

2027-05-07

Last updated by the study team

2026-04-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

• Cleveland Clinic - Weston Hospital — Weston, Florida, United States
• Cleveland Clinic - Ohio — Cleveland, Ohio, United States
• The Ohio State University — Columbus, Ohio, United States

Full record on ClinicalTrials.gov

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