drugset / Trial / NCT01205204

Comparison of Different Doses of Clonidine to Fentanyl as an Adjuvant to Bupivacaine 0.5% for Spinal Anesthesia

NCT01205204

RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to evaluate the safety, quality and duration of block with the addition of Clonidine in different doses to 0.5% heavy bupivacaine, and to compare it with addition of Fentanyl to 0.5% heavy bupivacaine in sub- arachnoid block.

Timeline

Start
2010-08
Primary completion
2011-07
Completion
2011-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Clonidine Other / unclassified 15 ug Other
Subject Clonidine Other / unclassified 30 ug Other
Subject Clonidine Other / unclassified 60 ug Other
Comparator Fentanyl Other / unclassified 25 ug Other

Indications

No indication recorded.