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NCT04079504

Comparison of Postoperative Pain After Hernial Sac Ligation Versus Non-ligation in Inguinal Hernioplasty

Completed NA Last updated 26 April 2022
What this trial tests

NA trial testing Ligation of indirect hernia sac in Inguinal Hernia, Indirect in 70 participants. Completed in 31 July 2021.

Timeline
1 October 2019
Primary endpoint
31 July 2021
31 July 2021

Quick facts

Lead sponsorDow University of Health Sciences
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment70
Start date1 October 2019
Primary completion31 July 2021
Estimated completion31 July 2021
Sites1 location across Pakistan

Drugs / interventions tested

Conditions studied

Sponsor

Dow University of Health Sciences

Who can join

15 and older, any sex, with Inguinal Hernia, Indirect or Postoperative Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is intends to compare mean postoperative pain scores for 48-hours in patients undergoing Inguinal hernioplasty with and without hernia sac ligation in Department of Surgery, Dow University of Health Sciences \& Dr. Ruth K. M. Pfau Civil Hospital Karachi.Half of the patients undergoing inguinal hernioplasty will have their indirect inguinal sacs ligated whereas other half will have non-ligation and inversion of sac.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Dow University of Health Sciences trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04079504.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing