Trial intelligence / Profile preview

Comparison of Bupivacaine vs Ropivacaine for Low Volume US-ISB

NCT02643563Completed

Sponsor
Sunnybrook Health Sciences Centre
Start
Jan 2016
Primary completion
Mar 2019
Modality
Orthosteric Ligands
Countries
1
01

Overview

Randomised, double-blind trial of ropivacaine and bupivacaine in postoperative pain (3 arms), sponsored by Sunnybrook Health Sciences Centre. Primary endpoint: Duration of analgesic block at 48 hours. Started Jan 2016; status: completed.

02

Drugs

ropivacainebupivacaine
03

Conditions

postoperative pain

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