drugset / Trial / NCT01205204
Comparison of Different Doses of Clonidine to Fentanyl as an Adjuvant to Bupivacaine 0.5% for Spinal Anesthesia
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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.