Clinical trial
Inguinal Hernia Study Using Biodesign IHM
NCT00393887 · Cook Group Incorporated, Industry · Completed
Key facts
| NCT number | NCT00393887 |
|---|---|
| Title | Inguinal Hernia Study Using Biodesign IHM |
| Official title | Inguinal Hernia Study: A Double Blinded Randomized Prospective Study |
| Lead sponsor | Cook Group Incorporated, Industry |
| Collaborators | Cook Biotech Incorporated Industry MED Institute, Incorporated |
| Status | Completed |
| Study type | Interventional |
| Conditions | Inguinal Hernia |
| Intervention type | Device |
| Interventions | Biodesign IHM, Polypropylene mesh |
| Enrollment | 100 |
| Start date | Mar 1, 2007 |
| Primary completion | Jun 1, 2014 |
| Completion | Jun 1, 2014 |
| First posted | Oct 30, 2006 |
| Last update posted | Nov 20, 2015 |
| Countries | United States |
At a glance
- 1–9 Study sites
- Yes Results posted
- 10–99 Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: