A clinical trial to compare the outcome of ultralight weight and lightweight mesh in inguinal hernia surgery

A comparative study of the outcome of ultralight weight and light weight polypropylene mesh in Lichtenstein repair of inguinal hernia - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/01/101234

Enrollment

Registered

2026-01-15

Start date

Unknown

Completion date

Unknown

Last updated

2026-02-02

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

Interventions

Intervention1: hernioplasty with ultralight weight mesh: Lichtenstein repair of inguinal hernia with ultralight weight mesh Control Intervention1: hernioplasty with light weight mesh: Lichtenstein rep

Eligibility

Inclusion criteria

Inclusion criteria: unilateral or bilateral inguinal hernia

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
1. PAIN AND DISCOMFORT 2. RECURRENCETimepoint: 2 years	—

Secondary

Measure	Time frame
nilTimepoint: nil	—

Countries

India

Contacts

Public ContactEkansh Hemant Singh

Ganesh Shankar Vidyarthi Memorial Medical College

rksingh.surg@mail.com8572917122

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026