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Comparison of Pruritus Incidence After Intrathecal Morphine 0.1 vs 0.2 mg in Cesarean Section

Name: Comparison of Pruritus Incidence After Intrathecal Morphine 0.1 vs 0.2 mg in Cesarean Section — clinical trial record (NCT07054775)
Creator: DataLookout
License: https://creativecommons.org/licenses/by/4.0/

StatusRecruiting

PhasePhase 4

SponsorKhon Kaen University

Started2025-06-01

View on ClinicalTrials.gov ↗

Record status

This record was last updated July 8, 2025 (before its estimated October 31, 2025 completion). Its status may not reflect the trial's current state.

Khon Kaen University

9 trials monitored

See 1 trial at risk

This study compares the incidence of pruritus (itching) requiring treatment between two doses of intrathecal morphine (0.1 mg vs 0.2 mg) when used for spinal anesthesia during cesarean section. The study aims to determine if the lower dose (0.1 mg) can reduce pruritus incidence while maintaining adequate pain relief.

Trial Details

NCT Number	NCT07054775
Lead Sponsor	Khon Kaen University
Conditions	Pruritus Caused by Drug
Enrollment	69 participants
Start Date	2025-06-01
Primary Completion	2025-10-31 (estimated)
Study Completion	2025-11-30 (estimated)
Updated on ClinicalTrials.gov	2025-07-08