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Clinical Trials/IRCT2014031717039N1
IRCT2014031717039N1
Completed
未知

Clinical trial of Comparison of low-dose Midazolam and Propofol on nausea and vomiting induced during operation, in pregnant women undergoing cesarean section with spinal anesthesia

Vice chancellor for research, Jahrom University of Medical Sciences0 sites42 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Vice chancellor for research, Jahrom University of Medical Sciences
Enrollment
42
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Vice chancellor for research, Jahrom University of Medical Sciences

Eligibility Criteria

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

Outcomes

Primary Outcomes

Not specified

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