Study to compare management of Incisional Hernia by two different types of mesh repair
Not Applicable
- Conditions
- Health Condition 1: K432- Incisional hernia without obstruction or gangrene
- Registration Number
- CTRI/2020/04/024677
- Lead Sponsor
- Department of General Surgery
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) All patients with Incisional hernia
2) Willing to comply with Protocol, and provide informed consent
Exclusion Criteria
1) Patients with other coexisting ventral hernias like Umbilical, Spigelian etc.
2) Patients < 18 years
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Identification of risk factors leading to Incisional hernia, preoperatively, which could help in correcting any modifiable risk factors in these patients, thus reducing the occurrence of Incisional Hernia.Timepoint: Till the end of study
- Secondary Outcome Measures
Name Time Method Identification of intra-operative findings and outcomes, which will help in making decision of <br/ ><br>which placement of mesh repair to use <br/ ><br>â?¢ Thus improving surgical outcome <br/ ><br>â?¢ Preventing major complications, which could reduce postoperative morbidity.Timepoint: Till the end of study