Prosthetic material (Mesh) anchored by mechanical device versus glue during laparoscopic repair of abdominal wall hernia: A double blind randomised control trial
Phase 3
- Conditions
- Health Condition 1: null- Primary ventral hernia
- Registration Number
- CTRI/2018/01/011268
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All consecutive patients (adult male and females > 18 and <65 years old) admitted for elective laparoscopic repair of primary ventral hernia.
Exclusion Criteria
1. Defect size less than 1 cm and greater than 5 cm on pre-operative ultrasound.
2. Secondary hernias including insicional hernia or parastomal hernia
3. Non midline ventral hernia
4. Patients with ASA grade IV and V
5. Significant co-morbidities like coronary artery disease, asthma, COPD, and previous
malignancy.
6. Patients requiring other concomitant procedures.
7. Patients who do not give consent for participation in the study or patient with
cognitive impairments
8. Patients on chronic analgesic use
9. Patients with uncorrectable coagulopathy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method