NCT06884826

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
150

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Aug 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 20, 2024

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

March 13, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

March 19, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 10, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 10, 2025

Completed
Last Updated

July 17, 2025

Status Verified

July 1, 2025

Enrollment Period

11 months

First QC Date

March 13, 2025

Last Update Submit

July 16, 2025

Conditions

DesardaComplicatedInguinal Hernia

Outcome Measures

Primary Outcomes (1)

  • Incidence of postoperative complications

    Incidence of postoperative complications such as groin pain, hemorrhage, infection, seroma, orchitis, and testicular atrophy will be recorded.

    24 hours postoperatively

Secondary Outcomes (2)

  • Stop of postoperative analgesic

    6 days postoperatively

  • Incidence of recurrence

    1 year postoperatively

Study Arms (1)

Desarda technique group

EXPERIMENTAL

Patients will undergo Desarda technique.

Procedure: Desarda technique

Interventions

Desarda techniquePROCEDURE

Patients will undergo Desarda technique.

Desarda technique group

Eligibility Criteria

Age14 Years+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Minia University

Minya, 61611, Egypt

Location

MeSH Terms

Conditions

Hernia, Inguinal

Condition Hierarchy (Ancestors)

Hernia, AbdominalHerniaPathological Conditions, AnatomicalPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer of General Surgery, Faculty of Medicine, Minia University, Minia, Egypt.

Study Record Dates

First Submitted

March 13, 2025

First Posted

March 19, 2025

Study Start

August 20, 2024

Primary Completion

July 10, 2025

Study Completion

July 10, 2025

Last Updated

July 17, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will share

The data will be available upon a reasonable request from the corresponding author after the end of study for one year.

Shared Documents
STUDY PROTOCOL
Time Frame
After the end of study for one year.
Access Criteria
The data will be available upon a reasonable request from the corresponding author.

Locations

EG(1)