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NCT03039426

Postoperative Cesarean Delivery Pain Relief; Diclofenac Versus Bupivacaine

Completed Phase 4 Last updated 22 October 2020
What this trial tests

Phase 4 trial testing Bupivacaine in Cesarean Delivery in 120 participants. Completed in 30 December 2017.

Timeline
1 January 2017
Primary endpoint
30 June 2017
30 December 2017

Quick facts

Lead sponsorDepartment of Medical Services Ministry of Public Health of Thailand
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposeprevention
Enrollment120
Start date1 January 2017
Primary completion30 June 2017
Estimated completion30 December 2017
Sites2 locations across Thailand

Drugs / interventions tested

Conditions studied

Sponsor

Department of Medical Services Ministry of Public Health of Thailand

Who can join

Adults 20 to 50, female only, with Cesarean Delivery. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This randomized controlled trial, compared postoperative pain score in patient undergoing cesarean delivery between bupivacaine peritoneal and subcutaneous infiltration and diclofenac intramuscular injection

Publications & conference data

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

Verify or expand the search:

Other trials of Bupivacaine

Trials testing the same drug.

Other recruiting trials for Cesarean Delivery

Currently open trials in the same condition.

Other Department of Medical Services Ministry of Public Health of Thailand 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/NCT03039426.

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