SUTURE REAIR- OPEN V/S KEYHOLE SURGERY FOR UMBILICAL HERNIA REPAIR

OPEN ANATOMICAL REPAIR V/S LAPAROSCOPIC REPAIR OF UMBILICAL HERNIA USING NO.1 POLYDIOXANONE SUTURE (PDS), RANDOMIZED CONTROL TRIAL.

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/01/017065

Enrollment

Registered

2019-01-14

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: K420- Umbilical hernia with obstruction,without gangrene

Interventions

Intervention1: Open anatomical repair: The patient is placed in the supine position with the left arm tucked alongside the patient. A first-generation cephalosporin is administered intravenously. Afte

Eligibility

Inclusion criteria

Inclusion criteria: 1.Written informed consent 2.Age group- more than 18 years 3.Umbilical hernia with defect size of

Exclusion criteria

Exclusion criteria: 1. Patients with obstructed or strangulated umbilical hernia 2. Patients with recurrent umbilical hernia.

Design outcomes

Primary

Measure	Time frame
Intraoperative timeTimepoint: From the time of 1st incision till closure of all port sites.	—

Secondary

Measure	Time frame
Postoperative pain, CosmesisTimepoint: Patient will be followed up for 6 months for above mentioned points and follow up visits will be at 72 hours, 1 week, 6 week, 6 months by OPD visits or telephonic visits.	—

Countries

India

Contacts

Public ContactDrRahul Kenawadekar

Jawaharlal Nehru Medical College

dr.rahuldk@gmail.com8970638114

Outcome results

None listed

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