Open Inguinal Hernia Repair With Mesh,the Use of Absorbable Versus Non Absorbable Fixation Sutures

Status

Withdrawn

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01467830

Enrollment

Registered

2011-11-09

Start date

2011-12-31

Completion date

2014-03-31

Last updated

2014-07-04

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

Conditions

Inguinal Hernia

Keywords

absorbable sutures efficacy, reducing Adverse effect to be caused from surgery, Inguinal Hernia repair with mesh

Brief summary

The purpose of this study is to determine the efficacy of mesh fixation using absorbable versus non-absorbable sutures.

Interventions

PROCEDUREOpen Inguinal Hernia Repair With Mesh,the Use of Absorbable Versus Non Absorbable Fixation Sutures

use of absorbable sutures to fixate mesh inguinal hernia repair.

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

SINGLE (Subject)

Eligibility

Sex/Gender

ALL

Age

18 Years to 90 Years

Healthy volunteers

Inclusion criteria

* all patients undergoing initial unilateral Open Inguinal Hernia Repair surgery.

Exclusion criteria

* patients having repeated Inguinal Hernia or bilateral Hernia * patients undergoing laparoscopic surgery.

Design outcomes

Primary

Measure	Time frame	Description
Impact of absorbable sutures in inguinal hernia repair on hernia recurrence and post operative outcome	two years	Absorbable sutures efficacy will be assessed according to:severity of post surgical pain(using NRS-Numerical Rating Scale measure),hernia recurrence (assessed by physical examination during the follow-up period) and other post surgical complications such as nerve entrapment,hematoma and stich granuloma

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026