drugset / Trial / NCT01224145

Assess the Feasibility and Efficacy of the CollaRx® Bupivacaine Implant Laparoscopic Inguinal or Umbilical Herniorrhaphy

NCT01224145

Phase 2 Completed 10 enrolled Innocoll Premier Research · collab
NaSingle-groupOpen-labelTreatment

Summary

This study will assess pain intensity for the first 72 hrs after aggravated movement (cough) following Laparoscopic Inguinal or Umbilical Herniorrhaphy.

Timeline

Start
2011-03-22
Primary completion
2011-06-20
Completion
2011-06-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Bupivacaine Other / unclassified 200 mg

Indications

No indication recorded.