KCT0008667
Recruiting
未知
Comparison of efficacy and safety of remimazolam and propofol: multicenter prospective randomized trial
Yonsei University Health System, Gangnam Severance Hospital0 sites394 target enrollmentTBD
ConditionsDiseases of the digestive system
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Diseases of the digestive system
- Sponsor
- Yonsei University Health System, Gangnam Severance Hospital
- Enrollment
- 394
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\) Men or women between the ages of 20 and 70
- •2\) Subjects who have voluntarily decided to participate after hearing the explanation of the clinical trial process and signed the consent form
- •3\) All subjects requiring ultrasound endoscopy
- •4\) Subjects with class I or II in the American Society of Anesthesiology (ASA) risk assessment
Exclusion Criteria
- •1\) Pregnant woman
- •2\) Those who are susceptible to remimazolam, propofol or benzodiazepine drugs (midazolam), or those who are susceptible to eggs, beans, etc
- •3\) subjects undergoing adrenocortical or chronic steroid therapy or porphyria
- •4\) Subjects who are expected to have difficulty with airway intubation (subjects who have difficulty opening their mouths wide or have a thick neck and short neck)
- •5\) a subject diagnosed with sleep apnea
- •6\) Subjects with a history of reported risk cases during sedative endoscopy in the past
- •7\) Subjects with severe renal disease (serum creatinine \>2 mg/dL)
- •8\) Subjects with severe heart disease (subjects with NYHA class III or IV)
- •9\) subjects who wish to receive an endoscopy without sincerity
- •10\) Subjects who cannot or are not willing to prepare an automatic test protocol or who do not agree to provide information;
Outcomes
Primary Outcomes
Not specified
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