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NCT00500214 Clinical Trial

Ilioinguinal Nerve Excision in Open Mesh Repair of Inguinal Hernia,a Randomized Clinical Trial

Postoperative Pain Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00500214
Other study ID # Ilioinguinal nerve excision
Secondary ID
Status Completed
Phase Phase 2
First received July 10, 2007
Last updated July 11, 2007
Start date April 2005
Est. completion date June 2007

Study information
Verified date July 2007
Source hahid Beheshti University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority Iran: Ministry of Health
Study type Interventional

Clinical Trial Summary

this study was designed to evaluate the effect of routine excision of the ilioinguinal nerve in an attempt to decrease the incidence of chronic inguinodynia in patients who undergo open anterior hernia mesh repair.

Description:

As chronic pain is the 2nd most common complication following open hernia repairs and it causes limitations and dysfunctions for the patients and also according to some previous studies elective ilioinguinal neurectomy could result in less postoperative pain,we decided to perform a randomized double blind clinical trial.The primary goal of this study was evaluation of the effect of this type of neurectomy on postoperative pain and hyposthesia.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date June 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- having an age of over 18 years

Exclusion Criteria:

- Those with diabetes, incarcerated, bilateral and recurrent hernias and visual problems were excluded from the investigation.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Prevention

Related Conditions & MeSH terms

Intervention

Procedure:
• elective ilioinguinal nerve excision

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
hahid Beheshti University of Medical Sciences

Outcome
Type Measure Description Time frame Safety issue
Primary postoperative pain using VAS (visual analogue scale) 1 year
Secondary postoperative hyposthesia using VAS (visual analogue scale) 1 year
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