CompletedNot Applicable

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

Thailand60 participantsStarted 2009-05

Plain-language 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.

Who can participate

Age range18 Years – 40 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * patient schedule for cesarean section ASA class 1 Exclusion Criteria: * have contraindication for spinal block * complicated pregnancy * have history of drug abuse during pregnancy * obesity BMI\>35kg./m2

What they're measuring

efficacy of intrathecal naloxone 0.4mg. in prophylaxis of intrathecal morphine induced pruritus after cesarean section

Timeframe: 24 hour

Trial details

NCT IDNCT00890942

SponsorMahidol University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2009-10

View on ClinicalTrials.gov More Morphine Adverse Reaction trials