Preventive Analgesia with Paracetamol for Post-Cesarean Section Pain Control
Not Applicable
Completed
- Conditions
- postoperatve pain after cesarean section.Other complications of obstetric surgery and procedures
- Registration Number
- IRCT201211187013N2
- Lead Sponsor
- Women's Reproductive Research Center, Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
Term parturients; Parturients with over 18 years; Parturients undergoing elective cesarean section with spinal anesthesia.
Exclution criteria:
To have a contraindication for spinal anesthesia; To have allergy to local anesthetics; Patients with mental disorders; Patients with organic dysfunctions; Previous chronic pain; Rased hepatic enzyms.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: PACU, every 1 hour until 4 hours and then every 4 hours until 24 hours after operation. Method of measurement: Visual analogue scale (VAS) from 0 (without pain) to 10 (severe and intolerable pain).
- Secondary Outcome Measures
Name Time Method Analgesic requirements. Timepoint: PACU, every 1 h until 4 h and then every 4 h until 24 h after operation. Method of measurement: Injection number and injection dose in mg.