A comparison of sedation with midazolam and remifentanil or dexmedetomidine and remifentanil during sling procedure
Not Applicable
- Conditions
- Diseases of The genitoruinary system
- Registration Number
- KCT0000159
- Lead Sponsor
- Asan Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Female
- Target Recruitment
- 50
Inclusion Criteria
1) scheduled for elective transobturator sling procedure for the treatment of urinary incontinence
2) female patient, 21 ~ 65 years old
3) volunteer for present clinical study
Exclusion Criteria
1) the patient who do not agree to participate in present study
2) allergic history for midazolam, opioids, or dexmedetomidine
3) bradycardia (<50 bpm) hypotension (SBP <90 mmHg)
4) 2 or 3 degree heart block, acute myocardial ischemia, heart failure
5) drug addction history
6) pregnancy, hepatic or reneal disease
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Bispectral Index;Recovery degree - Observer’s Assessment of Alertness/Sedation Scale(OAA/S);pain score (numeric rating score)
- Secondary Outcome Measures
Name Time Method end tidal CO2;vital sign (blood pressure, heart rate, oxygensaturation);patient satisfaction;operator satisfaction