Clinical trial of comparison of intrathecal with intravenous Dexamethasone to reduce post operation complications after cesarean sectio
Phase 2
- Conditions
- Single delivery by caesarean section.Delivery by elective caesarean section
- Registration Number
- IRCT2016112631095N1
- Lead Sponsor
- Vice chancellor for research, Mazandaran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
Inclusion criteria includes informed consent and undergoing elective cesarean section. Exclusion criteria includes unwillingness of the patient to continue participating in the study, height less than 150 cm, mental Disorders, corticosteroid use, alcohol consumption and drug abuse, contraindication to receive regional anesthesia, allergy to drugs used in the study, diabetes, hypertension and receiving antiemetic medications 24 hours prior to surgery
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ausea and vomiting. Timepoint: Recovery and then at 1, 6, 12 and 24 hours after discharge from recovery. Method of measurement: VAS.;Itching. Timepoint: Recovery and then at 1, 6, 12 and 24 hours after discharge from recovery. Method of measurement: VAS.;Pain. Timepoint: Recovery and then at 1, 6, 12 and 24 hours after discharge from recovery. Method of measurement: VAS.
- Secondary Outcome Measures
Name Time Method Patient Satisfaction. Timepoint: After discharge from recovery. Method of measurement: Visual analog scale.