Actively Recruiting
Comparison of Different Doses of Dexmedetomidine Combined With Ketamine for Post-Operative Pain Control in Cesarean Section Surgeries
Led by Fatima Memorial Hospital · Updated on 2025-06-18
90
Participants Needed
1
Research Sites
2 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to compare three different doses of dexmedetomidine combined with a fixed dose of ketamine for pain control in women undergoing cesarean section. It seeks to identify the most effective combination that provides good pain relief with the fewest side effects. The study focuses on managing postoperative pain, which can affect recovery, mother-child bonding, psychological well-being, and nursing after cesarean delivery. Participants will receive one of three continuous intravenous infusions during the postoperative period: dexmedetomidine at 0.2, 0.3, or 0.4 g/kg/hr combined with ketamine at a fixed dose of 0.25 mg/kg/hr. This combination is being studied because it may offer better pain relief with fewer opioid-related side effects, such as respiratory depression and nausea. The study will monitor the effects of these dosing regimens to determine optimal pain management. During the study, women's postoperative pain will be assessed using pain scores over the first 24 hours after surgery. Researchers will also track the time until first additional pain medication is needed and the total amount of rescue analgesia used within 24 hours. Safety and side effects will be monitored, and participants' responses will help guide improved protocols for pain control after cesarean section. The total participation period covers the immediate 24-hour postoperative phase.
CONDITIONS
Brief Title
Comparison of Dexmedetomidine + Ketamine for Postoperative Pain in C-Section
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Elective lower segment cesarean section
- American Society of Anesthesiologists (ASA) Physical Status II
- Provided informed consent
- Female
- Aged 18 to 50 years
You will not qualify if you...
- Known drug allergy
- Presence of significant comorbidities
- Emergency surgery
- Documented psychiatric illness
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 24 hours post-surgery
Participants receive continuous intravenous infusions of ketamine combined with varying doses of dexmedetomidine during the postoperative period following cesarean section surgery for pain control.
1 infusion period lasting up to 24 hours after surgery
Trial Site Locations
Total: 1 location
1
Department of Anesthesiology, Fatima Memorial Hospital
Lahore, Punjab Province, Pakistan, 54000
Actively Recruiting
Research Team
A
Ahmed Naeem, MBBS
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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