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Comparative study of mesh fixation in patients who have hernia of abdominal wall

A clinical trial to study the outcomes of non-absorbable versus absorbable tacker fixation of mesh in laparoscopic repair of incisional and ventral hernia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/06/005846
Enrollment
74
Registered
2015-06-03
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- ASA 1/2 pateints with primary ventral or incisional hernia

Interventions

Intervention1: Laparoscopic Mesh repair for incisional/ventral hernia and mesh fixation with either absorbable or non-absorbable tackers: Laparoscopic Mesh repair for incisional/ventral hernia and mes

Sponsors

All India Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Hernia defect size less than or equal to 15 cms. 2. Primary ventral hernia / umbilical hernias 3. Incisional hernias not operated upon earlier

Exclusion criteria

Exclusion criteria: 1. Recurrent hernias. 2. Defect size more than 15 cms 3. Patients with active skin infections. 4. Patients with significant co-morbidities like hypertension, tuberculosis, diabetes mellitus, and bronchial asthma. 5. Patients with any co-existing intra-abdominal pathology like gall stone disease, fibroids, intra-abdominal cysts, etc 6. Patients unfit for general anesthesia. 7. Patients with uncorrectable coagulopathy. 8. Patients not giving consent

Design outcomes

Primary

MeasureTime frame
To compare the incidence of early postoperative pain and chronic pain, recurrencerate, quality of life, return to physical activity, patient satisfaction,cosmetic outcome, cost effectiveness following following two techniques of mesh fixation- non-absorbable versus absorbable tackers - for laparoscopic mesh repair of incisional and ventral herniasTimepoint: Patients will be called at 1 week, 1 month, 3 months, 6 months, 12 months and yearly thereafter

Secondary

MeasureTime frame
To compare the incidence of postoperative complications. To compare the incidence of intraoperative complicationsTimepoint: Intra-operatively and post operatively

Countries

India

Contacts

Public ContactSridhar P

All India Institute of Medical Sciences, New Delhi, India

drvkbansal@gmail.com01126593686

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026