Status:
COMPLETED
Efficacy and Safety of Ciprofol for the Sedation in Patients Undergoing Hysteroscopy
Lead Sponsor:
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Conditions:
Ciprofol
Hysteroscopy
Eligibility:
FEMALE
18-65 years
Phase:
NA
Brief Summary
Eligible patients undergoing hysteroscopy were randomly assigned in a 1:1 ratio to receive intravenous anesthesia with either propofol (2 mg/kg) or remifentanil (0.4 mg/kg).Continuous monitoring of pu...
Eligibility Criteria
Inclusion
- Voluntary signing of informed consent form
- Stable vital signs and qualified anesthesia outpatient evaluation
- No contraindications to anesthesia
Exclusion
- Not willing to sign informed consent form
- Anaesthesia drug allergy
- Severe central nervous system diseases
- Severe hypertension and diabetes
- Mental disorders
- History of using psychotropic drugs in the past 3 months
Key Trial Info
Start Date :
January 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 30 2024
Estimated Enrollment :
124 Patients enrolled
Trial Details
Trial ID
NCT06172140
Start Date
January 1 2024
End Date
April 30 2024
Last Update
August 21 2024
Active Locations (1)
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1
Department of Anesthesiology, Sun Yat-sen Memorial Hospital, Sun Yat-sen Universit
Guangzhou, Guangdong, China, 510120