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Clinical Trial Active — Not Recruiting NCT07295379

LIQUIBAND FIX8® for Ventral Incisional Hernia

LIQUIBAND FIX8® for Ventral Incisional Hernia — Active Not Recruiting • NCT07295379.

📅 08 Jul 2026 ⏱ 2 min read
Active — Not Recruiting
Check the registry for current status and eligibility criteria.
Status
Active — Not Recruiting
NCT ID
NCT07295379
Start
2026-02-02
Completion
2026-07-30
ClinicaliQ Trial Snapshot
  • LIQUIBAND FIX8® for Ventral Incisional Hernia — Active Not Recruiting • NCT07295379.
  • Real-world safety and performance data on LiquiBand FIX8, a CE-marked adhesive device for securing mesh in ventral incisional hernia repair.

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What This Trial Is Studying

This study is designed to evaluate the safety and performance of device LiquiBand FIX8 Open hernia mesh fixation device. The use of this device is not experimental, as it is already approved for use in the EU (CE-marked). This is a retrospective post market clinical follow-up study to collect information about the use of the device in a real-world setting for ventral incisional hernia repair. Ventral incisional hernias occur following surgery and the most common method of treatment includes implanting a mesh, which in the case of ventral incisional hernia,…

Full Trial Details
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Eligibility criteria, protocol, and results when available
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