CompletedN/Aketamine
Effects of S-ketamine on Perioperative Opioid Consumption
Sponsored by Erasme University Hospital
NCT ID
NCT07528651
Target Enrollment
53 participants
Start Date
2021-06-07
Est. Completion
2022-06-21
About This Study
This study is a triple-blind randomized controlled trial conducted at a tertiary care hospital in Brussels. It investigates whether a single dose of S-ketamine can reduce opioid (morphine) consumption in the first 24 hours after elective laparoscopic gynecological surgery in relatively healthy adult patients (ASA 1-2). The goal is to assess S-ketamine's effectiveness within a standardized postoperative pain management protocol.
Conditions Studied
Interventions
- •Esketamine at low dose
- •Saline (0.9% NaCl)
Eligibility
Sex:FEMALE
Healthy Volunteers:Yes
View full eligibility criteria
Inclusion Criteria: * Adult patients American Society of Anesthesiologists (ASA) physical status classification I or II * Scheduled for elective laparoscopic gynecological surgery Exclusion Criteria: * Body mass index (BMI) \> 30 kg/m² * Known allergy to any drugs used in the study * Chronic pain patients or regular use of analgesics * Pregnant or breastfeeding patients
Study Locations (1)
Erasme Hospital
Brussels, Brussels Capital, Belgium