Clinical Trials Directory

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

TypeNameDescription
DRUGA single dose of 4 mg iv nalbuphineprevention 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.