Compare the Ketofol and Sodium thiopental in General anesthesia patients undergoing dilatation and curettage
Phase 2
- Conditions
- Surgical abortion.Complete or unspecified, complicated by delayed or excessive haemorrhage
- Registration Number
- IRCT2017031923559N9
- Lead Sponsor
- Vice chancellor for research, Ardabil University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Other
- Sex
- Female
- Target Recruitment
- 80
Inclusion Criteria
Vaginal bleeding; patients suspected to have an abortion; Patients candidate of uterine curettage; consent to participate in the study.
Exclusion criteria: contraindication to uterine curettage; sensitivity to Ketofol and Sodium thiopental
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Apnea. Timepoint: Intraoperative. Method of measurement: Based on the patient's respiratory status.
- Secondary Outcome Measures
Name Time Method Patient satisfaction of anesthesia. Timepoint: Intraoperative. Method of measurement: question of patient.;Decreased oxygen saturation. Timepoint: Intraoperative. Method of measurement: According to pulse oximetry.