Effects of Propofol or sodium thiopental on treatment outcomes in patients undergoing reproductive assisted technologies
Not Applicable
- Conditions
- Female infertility.Female infertility associated with male factors
- Registration Number
- IRCT201303135393N2
- Lead Sponsor
- Yazd University of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 90
Inclusion Criteria
(inclusion criteria: lack of infertility problems in the women and the presence of fertility problems in their husbands; Informed consent)
(Exclusion criteria: History of Hypertension; chronic respiratory diseases; thyroid disorders; severe side effects of drugs during the experiment)
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Systolic blood pressure. Timepoint: 5, 10, 15, 20 minutes after sedation. Method of measurement: mmHg.;Diastolic blood pressure. Timepoint: before sedation. Method of measurement: mmHg.;Heart rate. Timepoint: before sedation. Method of measurement: mmHg.;Respiratory rate. Timepoint: before sedation. Method of measurement: counting.;Rapid response to vocal stimulant. Timepoint: 5, 10, 15 and 20 minutes after anesthesia. Method of measurement: observation.;Vommiting. Timepoint: After Anesthesia. Method of measurement: Observation.
- Secondary Outcome Measures
Name Time Method