Status:
COMPLETED
Effectiveness of Low-Dose Ketamine and Intravenous Lidocaine Versus Fentanyl for Postoperative Pain
Lead Sponsor:
Dilla University
Conditions:
Postoperative Pain
Postoperative Nausea and Vomiting
Eligibility:
FEMALE
18-65 years
Phase:
PHASE4
Brief Summary
Background: Rational approaches to perioperative patient management have been used to meet intraoperative analgesic needs and avoid opioid-related adverse effects. A combination of drugs, such as keta...
Detailed Description
After obtaining ethical clearance from Dilla University College of Health Sciences and Medicine's ethics review board, a structured questionnaire will be developed and translated into the respective l...
Eligibility Criteria
Inclusion
- ASA I and II patients between the ages of 18 and 65 undergoing elective gynecologic surgery under general anaesthesia
Exclusion
- Patients with allergies to any of the drugs used in the trial Patients with chronic pain Patients who are diagnosed with CNS diseases like psychiatric diseases, epilepsy Patients who are hypertensive and taking beta blockers, as well as those who have preoperative bradycardia, hypotension, or any type of heart block, Breastfeeding and pregnant women Patients weighing less than 40 kg or obese patients (BMI \> 35 kg/m2) Patients with a history of smoking
Key Trial Info
Start Date :
June 10 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 20 2024
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT07213687
Start Date
June 10 2023
End Date
August 20 2024
Last Update
October 14 2025
Active Locations (1)
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1
Dilla University
Awasa, Snnpr, Ethiopia, 13