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The effect of Patient's position on post spinal anesthesia hypotensio

Not Applicable
Recruiting
Conditions
Hypotension & sensory block level during spinal anesthesia under different positions in c/s.
En Other complications of spinal and epidural anaesthesia during labour and delivery
Registration Number
IRCT20120915010841N13
Lead Sponsor
Hamedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
106
Inclusion Criteria

parturients aged 18 to 45 years old
Candidates for cesarean section under spinal anesthesia
ASA Physical Class 1 and 2

Exclusion Criteria

Heart disease
Hypertension
Eclampsia & pre-eclampsia
Diabetes
Those who are reluctant to continue to participate in the study
Patients who have failed spinal anesthesia and undergo general anesthesia
Spinal anesthesia Contraindications (High ICP, coagulation problems, shock, anemia)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Maximum sensory level. Timepoint: Every minute to 5 minutes. Method of measurement: Determination of sensory level by needle (Pinprick).;Onset time of sensory block. Timepoint: Every minute until the sensory block is fixed. Method of measurement: In minutes using the clock.;Systolic and Diastolic Blood Pressure. Timepoint: Every two minutes for 10 minutes and then every 10 minutes to 60 minute. Method of measurement: Non-invasive automatic barometric device.;Heart Rate. Timepoint: Every two minutes for 10 minutes and then every 10 minutes to 60 minute. Method of measurement: Non-invasive automatic barometric device.
Secondary Outcome Measures
NameTimeMethod
ausea and Vomiting. Timepoint: During surgery. Method of measurement: View and ask the patient.;Satisfaction. Timepoint: End of surgery. Method of measurement: Question from the patient.;Need for ephedrine. Timepoint: End of surgery. Method of measurement: Calculate consumed ephedrine.;Need for atropine. Timepoint: End of surgery. Method of measurement: Calculate consumed atropine.
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