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NCT03907813

Liposomal Bupivacaine After Cesarean Delivery

Withdrawn Phase 4 Last updated 31 July 2020
What this trial tests

Phase 4 trial testing Exparel in Pain, Postoperative. Withdrawn.

Timeline
1 May 2019
Primary endpoint
30 June 2020
31 July 2020

Quick facts

Lead sponsorWright State University
PhasePhase 4
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Start date1 May 2019
Primary completion30 June 2020
Estimated completion31 July 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Wright State University

Who can join

Adults 18 to 45, female only, with Pain, Postoperative or Opioid Use. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study is to determine if local wound infiltration with liposomal bupivacaine at the time of cesarean delivery can decrease opioid use and provide adequate post-operative pain control.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of Exparel

Trials testing the same drug.

Other recruiting trials for Pain, Postoperative

Currently open trials in the same condition.

Other Wright State University 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/NCT03907813.

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