Actively Recruiting

Phase 4
Age: 18Years - 50Years
FEMALE
NCT07022821

Comparison of Dexmedetomidine + Ketamine for Postoperative Pain in C-Section

Led by Fatima Memorial Hospital · Updated on 2025-06-18

90

Participants Needed

1

Research Sites

15 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Comparison of Dexmedetomidine + Ketamine for Postoperative Pain in C-Section

Who Can Participate

Age: 18Years - 50Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Elective lower segment cesarean section
  • American Society of Anesthesiologists (ASA) Physical Status II
  • Provided informed consent
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Department of Anesthesiology, Fatima Memorial Hospital

Lahore, Punjab Province, Pakistan, 54000

Actively Recruiting

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Research Team

A

Ahmed Naeem, MBBS

CONTACT

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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