drugset / Trial / NCT00656578

Efficacy and Safety Study of 4975 to Manage Pain of Bunionectomy

NCT00656578 ↗

Phase 3 Completed 300 enrolled Anesiva, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary purpose of this study is to compare the analgesic efficacy of a single intraoperative administration of 4975 vs. Placebo in the management of acute postoperative pain in patients undergoing bunionectomy. Secondary objective of this study is to evaluate the safety and tolerability of a single intraoperative administration of 4975.

Timeline

Start
2008-03
Primary completion
2008-08
Completion
2008-09

Drugs

EvaluationDrugModalityDoseRoute
Subject 4975 Unknown — —

Indications

No indication recorded.