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The Effect Of Ondansetron on maternal hypotension prevention during elective cesarean sectio

Not Applicable
Conditions
Maternal hypotension.
Maternal hypotension syndrome
Registration Number
IRCT201706015381N12
Lead Sponsor
Vice chancellor research for Babol University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
80
Inclusion Criteria

Inclusion Criteria: Pregnant women (18 to 35 years old) Candidate for elective cesarean section, In class I physical health classification of the American Society of Anesthesia. All women had singleton term pregnancies.

Exclusion Criteria

Mothers with a history of hypertension? Diabetes? cardiovascular and cerebral diseases? known fetal anomaly? any kind of contraindications for spinal anesthesia? psychosomatic Disorder? Patients weighting over 100 Kg and Height less than 150 cm and those with difficult tracheal intubation

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Maternal blood presure. Timepoint: Maternal blood pressure was monitored and recorded every two minutes for the first 15 minutes following spinal anesthesia, and then every 5 minutes until completion of surgery. Method of measurement: Non invasive blood presure cuff.
Secondary Outcome Measures
NameTimeMethod
Maternal heart rate. Timepoint: during surgery. Method of measurement: With cardiac monitoring and heart rate.;Neonatal arterial blood gas. Timepoint: After Surgery. Method of measurement: Arterial blood gas samples.;Neonatal apgar score. Timepoint: 1 and 5 minutes after surgery. Method of measurement: Cheklist/ examination/ observation.
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