drugset / Trial / NCT02591888

Impact of Liposomal Bupivacaine Administered Following Placement of a Transobturator Suburethral Sling

NCT02591888 ↗

Phase 4 Terminated 18 enrolled TriHealth Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Liposomal bupivacaine or placebo will be administered at the end of a transobturator midurethral sling to determine if there is a difference in a patient's perceived postoperative pain.

Timeline

Start
2015-02
Primary completion
2017-03
Completion
2017-12

Outcome

Outcome not reported

Stopped (Enrollment): “Difficult to enroll; since a similar research project on a different population showed no significance the study has been closed.”

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bupivacaine Other / unclassified 30 ml —

Indications

No indication recorded.