Effects of dexmedetomidine and propofol in adult patients
Not Applicable
Recruiting
- Conditions
- Congenital malformations, deformations and chromosomal abnormalities
- Registration Number
- KCT0000166
- Lead Sponsor
- Asan Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Patients aged from 21 to 65 undergoing device closure of cardiac septal defects assisted by fluoroscopy
Exclusion Criteria
1) The patient does not consent to participate in the study
2) Patients with a history of hypersensitivity reactions or side effects on propofol, opioid analgesics, or dekmedetomidin
3) bradycardia (less than 50 times per minute), hypotension (systolic blood pressure <90 mmHg)
4) second-degree or third-degree heart block, acute angina, congestive heart failure
5) patients who have drug dependence
6) pregnant women, or have liver or renal dysfunction
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method sedation state;satisfaction of patient and practitioner
- Secondary Outcome Measures
Name Time Method blood pressure;respiratory variable