Prophylactic Ilioinguinal Neurectomy During Open Tension-Free Inguinal Hernia Repair

Hernioplasty Clinical Trial

Official title:

Prophylactic Ilioinguinal Neurectomy During Open Tension-Free Inguinal Hernia Repair for Prevention of Chronic Postoperative Pain

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06327763
• Other study ID #: Ilioinguinal Neurectomy
• Status: Completed
• Phase: N/A
• Start date: January 1, 2022
• Est. completion date: June 1, 2023

Study information

• Verified date: March 2024
• Source: Zagazig University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

postoperative chronic inguinal pain is a common postoperative complication after open inguinal hernia repair. Chronic inguinal pain is a common complication following open inguinal hernia repair. Ilioinguinal nerve entrapment is a common cause of this chronic pain which may adversely affect the patients' life. Ilioinguinal neurectomy seems to be beneficial in preventing such pain, but it carries the risk for numbness and hypoesthesia.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 196
• Est. completion date: June 1, 2023
• Est. primary completion date: June 1, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 16 Years to 80 Years

Eligibility

Inclusion Criteria:

• the study included all adult patients operated on for unilateral inguinal hernia by Lichtenstein tension-free mesh hernioplasty with or without ilioinguinal neurectomy.

Exclusion Criteria:

• patients with recurrent inguinal hernia, bilateral inguinal hernia repair, or huge inguinoscrotal hernia were excluded. Diabetic patients as well as, patients with suspected inguinal hernia recurrence at the time of the questionnaire were excluded.

Related Conditions & MeSH terms

• Hernia, Inguinal
• Hernioplasty

Intervention

Procedure:
• ilioinguinal nerve section
patients operated on by open inguinal hernioplasty with ilioinguinal neurectomy

Locations

Country	Name	City	State
Egypt	yasmine Hegab	Zagazig

Sponsors (1)

Lead Sponsor	Collaborator
Zagazig University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	detect postoperative pain using short form inguinal pain questionnaire	ask the patient for presence of postoperative pain using short form inguinal pain questionnaire	3 months following operation then continous