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RANDOMISED CONTROLLED STUDY TO COMPARE INTRAPERITONEAL ONLAY MESH PLUS REPAIR VERSUS TRANSABDOMINAL PRE PERITONEAL MESH PLUS REPAIR FOR PATIENT WITH VENTRAL HERNIA

A PROSPECTIVE, RANDOMISED CONTROLLED STUDY TO COMPARE INTRAPERITONEAL ONLAY MESH PLUS REPAIR VERSUS TRANSABDOMINAL PRE PERITONEAL MESH PLUS REPAIR FOR PATIENT WITH VENTRAL HERNIA - IPOM PLUS VERSUS TAPP PLUS TRIAL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/041759
Enrollment
60
Registered
2022-04-08
Start date
Unknown
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

Health Condition 1: O- Medical and Surgical Health Condition 2: O- Medical and Surgical Health Condition 3: M95-M95- Other disorders of the musculoskeletal system and connective tissue

Interventions

Intervention1: IPOM PLUS VERSUS TAPP PLUS: GROUP 1: TAPP PLUS GROUP PROLENE MESH WILL BE PLACED EXTRAPERITONEALLY AFTER REDUCING THE CONTENTS OF HERNIA AND SUTURING THE DEFECT Group 2: IPOM PLUS GROU

Sponsors

ESIC Medical College and Hospital Faridabad
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age >= 18 years Ventral hernia (Primary or Incisional) Defect size 2-8 cm

Exclusion criteria

Exclusion criteria: 1. Patients undergoing emergency surgery 2. Parastomal or recurrent hernias 3. Unfit for General anesthesia and Laparoscopy

Design outcomes

Primary

MeasureTime frame
To compare postoperative morbidity including the pain scores and seroma rateTimepoint: 6hr, 24hr, 72 hr and than at 7, 30, 90, 180 and 360 days

Secondary

MeasureTime frame
To compare length of hospital stay, surgical site infection (SSI), hernia recurrence, mesh infection, cost, operative time and patient quality of life Timepoint: 6hr, 24hr, 72 hr and than at 7, 30, 90, 180 and 360 days

Countries

India

Contacts

Public ContactDr Devender Singh

ESIC MEDICAL COLLEGE AND HOSPITAL

devinderkuntal@gmail.com09813643337

Outcome results

None listed

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