Evaluating the Effect of Subcutaneous Dexamethasone Added to Bupivacaine on Postcesarean Pain Relief
Phase 4
- Conditions
- Complications of anaesthesia during pregnancy.Other complications of anaesthesia during pregnancy
- Registration Number
- IRCT138809242405N3
- Lead Sponsor
- Isfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 75
Inclusion Criteria
Inclusion Criteria: Parturients, ASA physical status I-II, scheduled for elective cesarean section, under general anesthesia.
Exclusion Criteria
patients with suspected or manifest bleeding disturbances, allergy to Bupivacaine or Dexamethasone, atopia, diabetes mellitus, the presence of liver or kidney diseases, abuse of drugs and patients with pregnant induced hypertension or preeclampsia.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain intensity. Timepoint: recovery room ,6 , 12, 24, 48 and 72 hours postoperative. Method of measurement: Visual Analogous Scale (VAS) and scoring from 0 to 10.
- Secondary Outcome Measures
Name Time Method Systolic blood pressure. Timepoint: at recovery room ,6 , 12, 24, 48 and 72 hours postoperative. Method of measurement: using mercury manometer.;Diastolic blood pressure. Timepoint: at recovery room ,6 , 12, 24, 48 and 72 hours postoperative. Method of measurement: using mercury manometer.;Opioid consumption. Timepoint: at recovery room ,6 , 12, 24, 48 and 72 hours postoperative. Method of measurement: mili gram of opioid.;Heart rate. Timepoint: at recovery room ,6 , 12, 24, 48 and 72 hours postoperative. Method of measurement: Using EKG Monitoring.