Actively Recruiting

Phase 4
Age: 18Years - 50Years
FEMALE
ID07022821

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

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
  • Female
  • Aged 18 to 50 years
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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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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

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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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