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NCT05549492

Transversus Abdominis Plane Block With or Without Buprenorphine After Inguinal Hernia Surgery

Completed Phase 1 Last updated 22 September 2022
What this trial tests

Phase 1 trial testing Ropivacaine 0.25%-NaCl 0.9% Injectable Solution in Inguinal Hernia in 64 participants. Completed in 30 May 2022.

Timeline
1 January 2021
Primary endpoint
1 May 2022
30 May 2022

Quick facts

Lead sponsorEgymedicalpedia
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment64
Start date1 January 2021
Primary completion1 May 2022
Estimated completion30 May 2022
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Egymedicalpedia — full company profile →

Who can join

Adults 30 to 45, any sex, with Inguinal Hernia or Pain, Postoperative. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Buprenorphine intravenous, sublingual, and transdermal patches have been researched for their antihyperalgesic effects, although peripherally mediated effects have not been examined in Egypt surprisingly

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Effect of transversus abdominis plane block with or without buprenorphine after inguinal hernia surgery on postoperative pain.
    Elshalakany NA, Salah AM. · · 2023 · cited 3× · PMID 38084572 · DOI 10.5114/ait.2023.132837

Verify or expand the search:

Other trials of Ropivacaine 0.25%-NaCl 0.9% Injectable Solution

Trials testing the same drug.

Other recruiting trials for Inguinal Hernia

Currently open trials in the same condition.

Other Egymedicalpedia trials

Trials by the same sponsor.

Verify against primary sources

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/NCT05549492.

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