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Clinical Trial Summary

One-thirds of patients underwent video-assisted thorascopic surgery still have severe pain. Therefore we want to demonstrate weather 0.15 mg spinal morphine would reduce 24 hour postoperative requirement comparing to control group.


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

  • Video-assisted Thoracoscopic Surgery

NCT number NCT01917448
Study type Interventional
Source Mahidol University
Contact
Status Completed
Phase Phase 4
Start date February 2014
Completion date January 2016

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