Trials / Withdrawn
WithdrawnNCT02730936
Antimicrobial Hernia Repair Device
Feasibility Study of the Antimicrobial Hernia Repair Device for Repair of Ventral or Incisional Hernia
- Status
- Withdrawn
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Cook Group Incorporated · Industry
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
This prospective early feasibility clinical study will collect information regarding the safety and efficacy of the Cook® Antimicrobial Hernia Repair Device to reinforce soft tissue during ventral or incisional hernia repair in clean-contaminated and contaminated (i.e., Class II and Class III) surgical fields.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Antimicrobial Hernia Repair Device | hernia repair |
Timeline
- Start date
- 2016-01-12
- Primary completion
- 2018-07-01
- Completion
- 2020-07-01
- First posted
- 2016-04-07
- Last updated
- 2017-02-13
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT02730936. Inclusion in this directory is not an endorsement.