Trials / Completed
CompletedNCT06837129
Intravenous Nalbuphine for Prevention of Intrathecal Morphine-induced Nausea and Vomiting in Patients Undergoing Cesarean Section: A Double-blind, Randomized Controlled Trial.
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 180 (actual)
- Sponsor
- Thammasat University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
We study efficacy of iv nalbuphine in prevention of intrathecal morphine-induced nausea and vomiting in patients undergoing cesarean section.
Detailed description
IV nalbuphine has been proved to help prevent intrathecal morphine-induced pruritus in some studies but results in nausea vomiting prevention have not been well studied. In Thailand, most caesarean section is done under spinal anesthesia with intrathecal morphine, proving that iv nalbuphine is effective would be beneficial for our population. This study aims to see whether 4 mg of nalbuphine is effective in reducing incidence of intrathecal morphine-related nausea vomiting in parturient who underwent C-section under spinal anesthesia with 0.2 mg of intrathecal morphine.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | A single dose of 4 mg iv nalbuphine | prevention of nausea vomiting |
Timeline
- Start date
- 2023-11-15
- Primary completion
- 2025-02-15
- Completion
- 2025-02-20
- First posted
- 2025-02-20
- Last updated
- 2026-01-28
Locations
2 sites across 1 country: Thailand
Source: ClinicalTrials.gov record NCT06837129. Inclusion in this directory is not an endorsement.