The effect of intravenous pump dexmedetomidine with paracetamol and ketorolac with paracetamol on pain after cesarean sectio

Phase 3

Recruiting

• Conditions: pain after cesarean section.; Acute pain, not elsewhere classified; G89.1

• Registration Number: IRCT20191025045237N1
• Lead Sponsor: Ahvaz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 5 January 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

Age between 18 to 40 years
ASA Class I and II
Candidate for elective cesarean section
No drug allergies to dexmedetomidine, ketorolac and paracetamol
Stable hemodynamics
Consent to participate in the study

Exclusion Criteria

history of asthma
history of bleeding or gastrointestinal ulcer
severe liver disease

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Severity of Pain. Timepoint: The time of 2, 4, 8, 12 and 24 hours after the surgery. Method of measurement: Visual analog scale (VAS).;Hemodynamics changes (Systolic and diastolic blood pressure, heart rate). Timepoint: The time of 2, 4, 8, 12 and 24 hours after the surgery. Method of measurement: Mercury barometer.

Secondary Outcome Measures

Name	Time	Method
ausea and vomiting. Timepoint: The time of 2, 4, 8, 12 and 24 hours after the surgery. Method of measurement: presence of nausea and vomiting based on direct observation and patients report.;Intensity of patients' anxiety. Timepoint: The time of 2, 4, 8, 12 and 24 hours after the surgery. Method of measurement: Ramsey sedate score (1-6).