Preemptive and Preventive Use of Paracetamol for Pain Relief After Cesarean Section
Phase 4
Completed
- Conditions
- Cesarean Section; Dehiscence
- Interventions
- Registration Number
- NCT02714179
- Lead Sponsor
- Baskent University
- Brief Summary
The investigators designed a prospective randomized study to investigate the efficacy of intravenous (IV) preemptive versus preventive paracetamol on postoperative pain scores, patient satisfaction, total morphine consumption and the incidence of morphine-related side effects in patients undergoing cesarean section.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 54
Inclusion Criteria
38 weeks pregnancy, elective cesarean section.
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Exclusion Criteria
morbid obesity, cardiac failure, depression.
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Group Preemptive (Group PE), Paracetamol was given intravenously in both group at different times Group I: i.V. paracetamol 1 g (100 ml) was given 30 min before induction of anesthesia. Group Preventive (Group PV), Paracetamol was given intravenously in both group at different times Group II: i.V. paracetamol 1 g (100 ml) was given before the end of surgery.
- Primary Outcome Measures
Name Time Method Visual analog score (VAS) for pain 24 hours
- Secondary Outcome Measures
Name Time Method