Actively Recruiting
Comparison of Pruritus Incidence After Intrathecal Morphine 0.1 vs 0.2 mg in Cesarean Section
Led by Khon Kaen University · Updated on 2025-07-08
69
Participants Needed
2
Research Sites
26 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Comparison of Pruritus Incidence After Intrathecal Morphine 0.1 vs 0.2 mg in Cesarean Section
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant women aged 18-45 years
- Full-term pregnancy
- Scheduled for non-emergency cesarean section
- ASA physical status I-III
- Non-complicated pregnancy
You will not qualify if you...
- Contraindication to spinal anesthesia or study drugs
- Refusal to participate in the study
- BMI 40 kg/m�b2 or higher
- History of systemic skin disease or current itchy skin condition
- Use of antihistamines or anti-pruritic medications within 3 days prior to surgery
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Faculty of Medicine, Khon Kaen University
Khon Kaen, Thailand, 40002
Actively Recruiting
2
Thepakorn Sathitkarnmanee
Khon Kaen, Thailand, 40002
Actively Recruiting
Research Team
T
Thepakorn Sathitkarnbmanee
CONTACT
S
Sirirat Tribuddharat
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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