Clinical Trials Directory

Trials / Completed

CompletedNCT00890942

Efficacy of Intramuscular Naloxone 0.4mg. in Prophylaxis of Intrathecal Morphine Induced Pruritus After Cesarean Section

Efficacy of Intramuscular Naloxone 0.4mg. in Prophylaxis of Intrathecal

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Mahidol University · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGnaloxonenaloxone 0.4mg.(1 ml) intramuscular
DRUGnormal salinenormal saline 1 ml IM

Timeline

Start date
2009-05-01
Primary completion
2009-10-01
Completion
2010-05-01
First posted
2009-04-30
Last updated
2011-07-25

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT00890942. Inclusion in this directory is not an endorsement.

Efficacy of Intramuscular Naloxone 0.4mg. in Prophylaxis of Intrathecal Morphine Induced Pruritus After Cesarean Section (NCT00890942) · Clinical Trials Directory