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Comparison of Midazolam and Propofol on nausea and vomiting induced during cesarean section with spinal anesthesia

Not Applicable
Conditions
ausea and vomiting.
Postprocedural disorder of digestive system, unspecified
Registration Number
IRCT2014031717039N1
Lead Sponsor
Vice chancellor for research, Jahrom University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
42
Inclusion Criteria

Inclusion Criteria: Written formal consent for operation, Pregnant women aged 15 to 60 years old, Class 1 and 2 ASA, Cesarean section candidate, No physical or mental illness, No consumption of Sedative, Antidepressant, Sleeping or Psychotropic medicine.

Exclusion Criteria

Weight more than 100 kg, Age more than 60 or less than 15, Drug or alcoholic abusers, Treatment by Anti depressant, sleeping and psychotropic pills, Inadequate cooperation with investigator to assess nausea and vomiting after operation, Hospitalization in ICU after operation, Any background of Propofol or Midazolam sensitivity, Need for additional treatment, Becoming ill after surgery, Increased anesthesia level, Respiratory distress, Patients of class 3 and 4 of ASA, Hemodynamic disorders

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ausea and Vomiting. Timepoint: 1 ,3, 5, 10, 15, 30 and 60 minutes after spinal anesthesia. Method of measurement: Have or not have with the Questionnaire made by Investigator.
Secondary Outcome Measures
NameTimeMethod
Blood pressure. Timepoint: 1, 3, 5, 10, 15, 30 and 60 minutes after spinal anesthesia. Method of measurement: Sphygmomanometer.;Pulse. Timepoint: 1, 3, 5, 10, 15, 30 and 60 minutes after spinal anesthesia. Method of measurement: Pulse oximetry.;Respiratory Rate. Timepoint: 1, 3, 5, 10, 15, 30 and 60 minutes after spinal anesthesia. Method of measurement: Counting breaths by investigator.;O2 Saturation of arterial blood. Timepoint: During surgery and recovery. Method of measurement: Pulse oximetry.;Apgar. Timepoint: 1 and 5 minutes after the birth. Method of measurement: Assessment by investigator by Apgar criteria.
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