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Clinical Trial Summary

This study aims to compare the efficacy of 0.05 mg and 0.1 mg spinal morphine in reducing postoperative morphine requirement in patients undergoing vaginal hysterectomy with/without anterior and posterior vaginoplasty.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01079754
Study type Interventional
Source Mahidol University
Contact Sirilak Suksompong, MD
Phone 6624113256
Email sisuk@mahidol.ac.th
Status Recruiting
Phase Phase 4
Start date March 2010
Completion date December 2011

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