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Intravenous nalbuphine for preventionof intrathecal morphine-induced nausea and vomiting in patients undergoing cesarean section : A double-blind, randomized controlled trial

Intravenous nalbuphine for prevention of intrathecal morphine-induced nausea and vomiting in patients undergoing cesarean section : A double-blind, randomized controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20241205001
Enrollment
180
Registered
2024-12-05
Start date
2024-12-05
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

intrathecal morphine-induced nausea and vomiting in patients undergoing cesarean section intrathecal morphine-induced nausea and vomiting, cesarean section

Interventions

nalbuphine 4 mg IV ,NSS 4 ml IV
Active Comparator Drug,Placebo Comparator No treatment
nalbuphine ,placebo

Sponsors

thammasat University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Elective cesarean section under spinal anesthesia 2. older than 18 years old

Exclusion criteria

Exclusion criteria: 1. Patients with known allergy to research drugs such as nalbuphine, bupivacaine or morphine 2. Medical complications eg heart diseases, diabetes, hypertension, renal or hepatic disease, obesity >=100 kilograms 3. Obstetrical complications eg twins or multiple gestation, pre-eclampsia, IUGR(intra-uterine growth retardation), placenta previa 4. History of postoperative nausea and vomiting (PONV), motion sickness or passive smoker 5. Patient with known history of drug abuse 6. Unwilling to participate in the study

Design outcomes

Primary

MeasureTime frame
event rate of nausea and vomiting postoperative 1,6,24 hr event rate

Secondary

MeasureTime frame
severity of nausea postoperative 1,6,24 hr nausea and vomiting score 0-3,severity of pruritus postoperative 1,6,24 hr pruritus score 0-3,sedation score postoperative 1,6,24 hr sedation score 0-3 ,pain score postoperative 6,24 hr Numeric pain score

Countries

Thailand

Contacts

Public ContactPreeyaphan Arunakul

Department of Anesthesiology, Faculty of Medicine, Thammasat University

kpreeyap@tu.ac.th0816635144

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026