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Intrathecal Versus Intravenous Dexmeditomedine in Transurethral Resection of the Prostate

Dexmedetomidine Clinical Trial

Official title:
The Effect of Intrathecal Versus Intravenous Dexmeditomedine on Postoperative Analgesia in Transurethral Resection of the Prostate

Clinical Trial Summary

This study is to evaluate The analgesic effect of intrathecal versus intravenous dexmeditomedine in transurethral resection of the prostate

Clinical Trial Description

This study will carried out in Tanta University hospital on75 male patients Patients will randomly classified into 3 groups Group I: will receive intrathecal hyperbaric bupivacaine 10mg in 2.5 ml and .5 ml saline with 3ml total volume Group II: will receive dexmeditomedine 5Mic diluted in.5 ml saline and hyperbaric bupivacaine 10mg in 2.5ml with 3ml total volume Group IIl: Will receive intravenous dexmeditomedine started at loading dose of 1 mic/kg diluted in 50 ml saline and administered within 10 min as loading dose , followed by maintenance at a dose of .4mic/kg/h diluted in200 ml saline till the end of surgery and hyperbaric bupivacaine 10 mg in 2.5 ml total volume ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04618965
Study type Interventional
Source Tanta University
Contact Laila ElAhwal, MD
Phone 00201018484319
Email lailaalahwal@gmail.com
Status Not yet recruiting
Phase Phase 4
Start date November 1, 2020
Completion date June 26, 2021
View Details
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