Trials / Active Not Recruiting
Active Not RecruitingNCT04059640
PMCF Study of LiquiBand FIX8® OHMF Device
PMCF Study to Evaluate the Safety and Performance of LiquiBand FIX8® Open Hernia Mesh Fixation Device
- Status
- Active Not Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 109 (actual)
- Sponsor
- Advanced Medical Solutions Ltd. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Study to evaluate the safety and performance of LiquiBand FIX8® Open Hernia Mesh Fixation Device.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | LiquiBand FIX8 Open Hernia Mesh Fixation Device | Subjects will undergo hernia mesh fixation and topical wound closure using the LiquiBand FIX8® OHMF device. Subjects will be evaluated intra-operatively, post-operatively, at discharge, and at 12 months post-operatively. The Liquiband surgical study device is considered a permanent implant. |
Timeline
- Start date
- 2021-12-07
- Primary completion
- 2025-07-31
- Completion
- 2026-07-31
- First posted
- 2019-08-16
- Last updated
- 2025-10-02
Locations
3 sites across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT04059640. Inclusion in this directory is not an endorsement.