The effect of dexmedetomidine and paracetamol on postoperative pain of cesarean section with spinal anesthesia

Phase 3

Recruiting

• Conditions: Acute postoperative pain.; Other acute postprocedural pain; G89.18

• Registration Number: IRCT20110712007013N27
• Lead Sponsor: Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 18 May 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 100

Inclusion Criteria

Pregnant women between the ages of 18 and 60 years old
ASA class one and two
Candidates for elective cesarean section or spinal anesthesia

Exclusion Criteria

Sensitivity to the compounds used for intervention group
Mental illness
Patients with cardiovascular, pulmonary, liver and kidney and ...disease
Multiple pregnancy
Urgent cesarean

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: At post-anesthesia care unit and at 1, 3, 6, 12 and 24 hours after surgery. Method of measurement: Visual analogue scale (VAS) (from 0= no pain to 10= severe pain).

Secondary Outcome Measures

Name	Time	Method
Overall dose of postoperative analgesic. Timepoint: At post-anesthesia care unit and during 24 hours after surgery. Method of measurement: Number and amount of medication by mg, based on patient's record.