Comparison of Dexmedetomidine + Ketamine for Postoperative Pain in C-Section
Recruiting
Phase 4
Interventional Study
Postoperative Pain
Cesarean Section Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 18 – 50
- Sex
- Female
- Trial phase
- Phase 4
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 90 (estimated)
- Sponsor
- Fatima Memorial Hospital · Other
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About This Trial
This study aims to compare three different doses of dexmedetomidine, when combined with a fixed dose of ketamine, for pain control in women undergoing cesarean section. The goal is to find the most effective combination with the fewest side effects.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Elective lower segment cesarean section
* American Society of Anesthesiologists (ASA) Physical Status II
* Provided informed consent
Exclusion Criteria:
* Known drug allergy
* Presence of significant comorbidities
* Emergency surgery
* Documented psychiatric illness
Contacts