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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03765268
Other study ID # s9
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2017
Est. completion date July 1, 2018

Study information

Verified date February 2019
Source Services Hospital, Lahore
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

It is a randomized controlled trial in which we are treating inguinal hernia patients with mesh hernioplasty and either neurectomy of iliohypogastric nerve and ilioinguinal neurectomy or preservation comparing post operative acute or chronic pain


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date July 1, 2018
Est. primary completion date July 1, 2018
Accepts healthy volunteers No
Gender Male
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria:

- patients male, and age between 20 to 70 years Reducible inguinal hernia

Exclusion Criteria:

- Irreducible, obstructed or strangulated hernia uncontrolled diabetes

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Neurectomy in inguinal hernia repair
Mesh hernioplasty of inguinal hernia with neurectomy of ilioinguinal and iliohypogastric nerve
nerve sparing in inguinal hernia repair
Mesh hernioplasty of inguinal hernia with sparing of ilioinguinal and iliohypogastric nerve

Locations

Country Name City State
Pakistan Services Hospital Lahore Lahore Punjab

Sponsors (1)

Lead Sponsor Collaborator
Services Hospital, Lahore

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary percentage of patients developing chronic inguinodynia Excruciating Pain measured by visual analog score (with 1 being minimum score and 10 being maximum score) for more than 3 months in inguinal region after open mesh hernioplasty for inguinal hernia 3 months
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