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Clinical Trial Summary

The purpose of this study is to determine whether intramuscular naloxone 0.4mg. is effective in prophylaxis of intrathecal morphine induced pruritus after cesarean section.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00890942
Study type Interventional
Source Mahidol University
Contact
Status Completed
Phase N/A
Start date May 2009
Completion date May 2010

See also
  Status Clinical Trial Phase
Recruiting NCT04052867 - Intravenous Lignocaine Infusion in Laparoscopic Donor Nephrectomy N/A
Not yet recruiting NCT05560542 - Intrathecal Dexamethasone and Atropine on Morphine Induced Post-operative Nausea and Vomiting on Caesarean Section N/A
Terminated NCT01844206 - Two Dose Epidural Morphine for Post-cesarean Analgesia Phase 4
Completed NCT03035942 - Quality of Recovery After Dexamethasone, Ondansetron or Placebo Intrathecal Morphine Administration Phase 4
Completed NCT01952626 - Prevention of Intrathecal Morphine Induced Pruritus: Comparison of Ondansetron and Palonosetron N/A