Evaluation of Desarda Technique in Management of Complicated Inguinal Hernia

Status

Completed

Phases

Unknown

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT06884826

Enrollment

150

Registered

2025-03-19

Start date

2022-08-01

Completion date

2025-07-31

Last updated

2026-05-19

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

Conditions

Complicated, Desarda, Inguinal Hernia

Brief summary

This study aims to evaluate the desarda technique in management of complicated inguinal hernia.

Detailed description

Desarda technique is one of the best surgical methods suitable for emergency hernia surgery repair, but there is still limited consensus. The purpose of this study is to assess the Long-term outcome of the pure tissue Desarda technique for the treatment of emergency inguinal hernias repair (Incarcerated, Irreducible, and Obstructed Patients) regarding Postoperative Complications, Groin Pain, and recurrence rate. Surgical techniques for emergency inguinal hernia surgery remain an important less documented area. Emergency inguinal hernia can have different presentations. Incarceration is characterized by the irreducibility of contents and strangulation by the compromise of the blood supply of the contents (e.g., bowel, omentum).

Interventions

PROCEDUREDesarda technique

Patients will undergo Desarda technique.

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

14 Years to No maximum

Healthy volunteers

Inclusion criteria

* Age above 14 years old. * Irreducible, incarcerated \& obstructed inguinal or inguinoscrotal hernia; unilateral or bilateral

Exclusion criteria

* Recurrent Hernias. * Intra-operative finding of separated thin and/or weak external oblique aponeurosis.

Design outcomes

Primary

Measure	Time frame	Description
Incidence of postoperative complications	24 hours postoperatively	Incidence of postoperative complications such as groin pain, hemorrhage, infection, seroma, orchitis, and testicular atrophy will be recorded.

Secondary

Measure	Time frame	Description
Stop of postoperative analgesic	6 days postoperatively	Stop of postoperative analgesic (Within 3 days, 3-6 day, More than 6 days) will be recorded.
Incidence of recurrence	1 year postoperatively	Incidence of recurrence will be recorded.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 20, 2026