drugset / Trial / NCT03385967

Duration of Analgesia With Dexmedetomidine and Ropivacaine in Brachial Plexus Block

NCT03385967 ↗

Phase 4 Withdrawn University of Florida
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a prospective, randomized, double blind study of adding dexmedetomidine to ropivacaine for Brachial plexus block and assessing the analgesia with VAS pain scales(0-10), Satisfaction scale by VAS scale(0-10) and time to first analgesic consumption. This study mainly aims to investigate whether addition of dexmedetomidine helps in increasing the duration of analgesia.

Timeline

Start
2019-04
Primary completion
2019-12
Completion
2019-12

Outcome

Outcome not reported

Stopped: “PI is leaving the University of Florida”

Drugs

EvaluationDrugModalityDoseRoute
Comparator Dexmedetomidine Other / unclassified 0.25 ug/kg Other
Comparator Ropivacaine Other / unclassified 0.5 % Other
Comparator Ropivacaine Other / unclassified 25 ml Other

Indications

No indication recorded.