Comparison of the effects of two different doses of dexmedomidine and propofol in sedation during ovarian surgery
Phase 3
Not yet recruiting
- Conditions
- Ovarian puncture surgery.
- Registration Number
- IRCT20200825048515N73
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 96
Inclusion Criteria
Infertile women candidates for puncture operation with IVF/ICSI indication
Age 25 to 43 years
With ASA I or II
Consent to enter the study
Exclusion Criteria
Having an allergy to any drug used
Having a history of diseases such as epilepsy and gastric reflux and a history of severe cardiovascular disease and the presence of atrial block or stroke
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sedation. Timepoint: Before the intervention and then 5, 10, 15 and 30 minutes after the intervention and then every 15 minutes during recovery until discharge. Method of measurement: Richmond sedation score scale (RASS) as a score of +4 to -5.;Hear rate. Timepoint: Before the intervention and then 5, 10, 15 and 30 minutes after the intervention and then every 15 minutes during recovery until discharge. Method of measurement: Monitoring device.;Diastolic blood pressure. Timepoint: Before the intervention and then 5, 10, 15 and 30 minutes after the intervention and then every 15 minutes during recovery until discharge. Method of measurement: Monitoring device.;Systolic blood pressure. Timepoint: Before the intervention and then 5, 10, 15 and 30 minutes after the intervention and then every 15 minutes during recovery until discharge. Method of measurement: Monitoring device.
- Secondary Outcome Measures
Name Time Method