Evaluation of the effect of elastic bandage on Post spinal hypotensio
Not Applicable
Recruiting
- Conditions
- Post spinal anesthesia hypotension in C/S.
- Registration Number
- IRCT20120915010841N23
- Lead Sponsor
- Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 64
Inclusion Criteria
Patients aged 18 to 46 years
With term pregnancy (37 weeks and more)
Physical Status (ASA) Class 1 and 2
Candidate for cesarean section under spinal anesthesia
Satisfaction to participate in the research
Exclusion Criteria
Patients with respiratory disease
Hypertension
Diabetes
Heart failure and cardiac arrhythmia
Multiple pregnancies
Eclampsia and preeclampsia
Emergency cesarean section
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Hypotension. Timepoint: Every two minutes to 10 minutes, then every 5 minutes to 15minutes, then every 10 minutes until the end of the surgery. Method of measurement: Automatic non-invasive blood pressure device.
- Secondary Outcome Measures
Name Time Method Systolic and Diastolic Blood Pressure. Timepoint: Every two minutes to 10 minutes, then every 5 minutes to 15 minutes, then every 10 minutes until the end of the surgery. Method of measurement: En Automatic non-invasive blood pressure device.;Heart Rate. Timepoint: Every two minutes to 10 minutes, then every 5 minutes to 15 minutes, then every 10 minutes until the end of the surgery. Method of measurement: pulse oximetry.;Nausea and Vomiting. Timepoint: During and after surgery. Method of measurement: Observation.;New born Apgar. Timepoint: 1&5 minutes after delivery. Method of measurement: Apgar Score.;The amount of ephedrine have been consumed. Timepoint: During surgery. Method of measurement: mg.;The amount of atropine have been consumed. Timepoint: During surgery. Method of measurement: mg.