Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07054775

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

Comparison of Pruritus Incidence After Intrathecal Morphine 0.1 and 0.2 Milligrams in Cesarean Section: A Randomized Clinical Trial

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
69 (estimated)
Sponsor
Khon Kaen University · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

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.

Detailed description

Spinal anesthesia is a standard technique for cesarean section. Intrathecal morphine (ITM) provides prolonged and effective analgesia but may cause adverse events including pruritus, nausea, vomiting, and respiratory depression. Current practice at Srinagarind Hospital uses ITM 0.2 mg for spinal anesthesia in cesarean section. This study investigates whether reducing the ITM dose to 0.1 mg can decrease pruritus incidence while preserving analgesic effectiveness.

Conditions

Interventions

TypeNameDescription
DRUGMorphine Sulfateintrathecal administered morphine

Timeline

Start date
2025-06-01
Primary completion
2025-10-31
Completion
2025-11-30
First posted
2025-07-08
Last updated
2025-07-08

Locations

2 sites across 1 country: Thailand

Source: ClinicalTrials.gov record NCT07054775. Inclusion in this directory is not an endorsement.