Effect of fluid therapy in reducing complications of spinal anesthesia
Phase 2
- Conditions
- Spinal anesthesia.Other complications of spinal and epidural anaesthesia during pregnancy
- Registration Number
- IRCT2013051612094N2
- Lead Sponsor
- Vice Chancellor for Research, Mashhad University of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Candidates for elective cesarean surgery; ASA I-II; 18-40 years old.
Exclusion criteria: Patients who received intravenous fluids before entering the operating room; BMI=30; ASA>3; Age less than 18 years and more than 40 years; Contraindications to spinal anesthesia procedures; Emergency cesarean section; Amount of intraoperative bleeding over 1000cc; History of hypertension and blood pressure in pregnancy; Instances may increase the risk of bleeding and inertia.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood pressure changes. Timepoint: Befor spinal, every 3 minutes to initial 10 minutes, and then every 5 minutes until recovery. Method of measurement: Perioperative monitoring.;Heart rate changes. Timepoint: Befor spinal, every 3 minutes to initial 10 minutes, and then every 5 minutes until recovery. Method of measurement: Perioperative monitoring.
- Secondary Outcome Measures
Name Time Method ausea & Vomiting. Timepoint: Postoperative time. Method of measurement: Clinical observation.;Chest discomfort. Timepoint: Duration of Surgery. Method of measurement: Recorded in the questionnaire.;Neonate apgar. Timepoint: Duration of Surgery. Method of measurement: Recorded in the questionnaire.;Efedrin require. Timepoint: Duration of Surgery. Method of measurement: Recorded in the questionnaire.