drugset / Trial / NCT01541059

Postoperative Analgesia Following Wisdom Teeth Removal: Ropivacaine Versus Placebo

NCT01541059 ↗

Phase 4 Completed 100 enrolled Nîmes University Hospital
RandomizedParallel-groupTriple-blindTreatment

Summary

The main objective of this study is to demonstrate the superiority of local analgesia with ropivacaine versus placebo on postoperative pain during the first 24 hours following bilateral surgery of all four third molars under general anesthesia.

Timeline

Start
2012-06
Primary completion
2015-08-29
Completion
2015-08-29

Outcome

Met primary endpoint

paper Area Under the Curve for VAS pain (0 to 4h) was lower for Ropivacaine group: 0.43 [0.19-0.66] vs. 0.63 [0.43-0.87], P=0.005. PMID 31326593 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Ropivacaine Other / unclassified 2 ml Other
Subject Ropivacaine Other / unclassified 7.5 mg/ml Other

Indications

No indication recorded.