Trials / Unknown
UnknownNCT02507830
Mesh Fixation With a Synthetic Glue in Primary Inguinal Hernia Repair
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 150 (estimated)
- Sponsor
- Rambam Health Care Campus · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Prospective observational study with mesh fixation using FDA approved synthetic glue,glubran 2 and standard mesh fixation with stiches in primary inguinal hernia repair surgery. The investigators aim is to recruit 150 patients for the study. The outcomes The investigators would like to determine are : postoperative pain,recurrences and complication rates such as seromas.
Detailed description
Prospective observational study with mesh fixation using FDA approved synthetic glue,glubran 2 and standard mesh fixation with stiches in primary inguinal hernia repair surgery. The investigators aim is to recruit 150 patients for the study. The outcomes The investigators would like to determine are : postoperative pain,recurrences and complication rates such as seromas.
Conditions
Timeline
- Start date
- 2015-08-01
- Primary completion
- 2017-07-01
- Completion
- 2017-07-01
- First posted
- 2015-07-24
- Last updated
- 2016-03-03
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT02507830. Inclusion in this directory is not an endorsement.