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

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00500214
Enrollment
Unknown
Registered
2007-07-12
Start date
2005-04-30
Completion date
2007-06-30
Last updated
2007-07-12

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

Conditions

Postoperative Hyposthesia, Postoperative Pain

Keywords

inguinal hernia, herniorrhaphy, mesh repair, ilioinguinal neurectomy, postoperative pain in cases and controls during one year., postoperative hyposthesia in cases and controls during one year.

Brief 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.

Detailed 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.

Interventions

PROCEDUREelective ilioinguinal nerve excision

Sponsors

Shahid Beheshti University of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
postoperative pain using VAS (visual analogue scale)1 year

Secondary

MeasureTime frame
postoperative hyposthesia using VAS (visual analogue scale)1 year

Outcome results

None listed

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