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
| Type | Name | Description |
|---|---|---|
| DRUG | Morphine Sulfate | intrathecal 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.