Opioid consumption, quality of pain control, complication and satisfaction in postoperative period of elective cesarean section Intrathecal morphine, Acetaminophen, COX-II inhibitor, Non-steroidal anti-inflammatory drugs, NSAIDs, Cesarean section
Conditions
Interventions
Paracetamol 1000 mg IV at recovery room then 1000 mg IV or oral q6h x 1 day,Parecoxib 40 mg IV at recovery room then 40 mg IV q12h x 1 day
Active Comparator Drug,Active Comparator Drug
Paracetamol group,Parecoxib group
Sponsors
None listed
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: 1. Female participant age 18-40 years old undergoing elective cesarean section 2. ASA II 3. BMI 18-40 kg/m2
Exclusion criteria
Exclusion criteria: 1. Patient deny 2. Unable to communicate with researcher 3. Medication allergy or contraindication to medication which will be administered in this study 4. Contraindication of spinal anesthesia 5. Chronic opioid user
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Opioid consumption 24 hours postoperative Collection from PCA machine | — |
Secondary
| Measure | Time frame |
|---|---|
| Time to first dose opioid rescue Time to first dose opioid rescue Collection from PCA machine,Pain score (NRS) 1,4,8,12,24 hours postoperative Questionaire,Rate of complication 24 hours postoperative Questionaire,Satisfaction score 24 hours postoperative Questionaire | — |
Countries
Thailand
Contacts
Public ContactDissakul Prasitreungsuk
King Chulalongkorn Memorial Hospital
Outcome results
None listed