Clinical Trials Directory

Trials / Completed

CompletedNCT06153602

Effectiveness of Nalbuphine as an Adjuvant to Subarachnoid Block on Postoperative Analgesia in TURP Surgery

Effectiveness of Intrathecal Nalbuphine as an Adjuvant to Subarachnoid Block on Postoperative Analgesia in Patients Undergoing Transurethral Resection of the Prostate

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Chulalongkorn University · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to compare pain after surgery in patients undergoing Transurethral Resection of Prostate. The main question it aims to answer are: Intrathecal nalbuphine as an adjuvant to local anesthetic will better provide pain relief after TURP surgery. Participants will be given a combination of nalbuphine and local anesthetic when getting a spinal block. Researchers will compare control group, given look-alike solution that contains no active drug to see if nalbuphine will better provide pain relief after surgery.

Detailed description

This study aims to evaluate the efficacy and side effects of nalbuphine, with the goal of providing anesthesiologists with evidence-based guidance for selecting the most appropriate pharmacological agents for their patients. Participants will be given a combination of nalbuphine and local anesthetic when getting a spinal block. Researchers will compare control group, given look-alike solution that contains no active drug to see if nalbuphine will better provide pain relief after surgery.

Conditions

Interventions

TypeNameDescription
DRUGNalbuphine Hydrochloride 10 MG/MLNalbuphine(10mg/ml) 0.8 mg intrathecal
DRUGSodium Chloride 0.9 % in 5 ML Injection0.9% Sodium Chloride 0.08 ml intrathecal
DRUGBupivacaine Hydrochloride, Spinal0.5% Hyperbaric or Isobaric Spinal Bupivacaine 1-4 ml intrathecal
DRUGNalbuphine Hcl 10Mg/Ml Inj4 mg IV prn for postoperative pain score\>=4 q 6 h
DRUGAcetaminophen 500Mg Tab1 tab oral prn for postoperative pain score 1-3 q 6 h
DRUGOndansetron 8mg8 mg IV prn for nausea or vomiting q 8 h

Timeline

Start date
2023-12-07
Primary completion
2024-11-27
Completion
2024-11-28
First posted
2023-12-01
Last updated
2025-01-13

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT06153602. Inclusion in this directory is not an endorsement.