Last updated: June 6, 2023
Sponsor: Le Yu
Overall Status: Active - Recruiting
Phase
N/A
Condition
Anesthesia
Treatment
Propofol injection
ciprofol injection
Clinical Study ID
NCT05892471
2022.8.1-2023.8.1
Ages 55-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Elective surgery patients
- Aged 55 to 75
- New York Heart Association class II or III cardiac functions
- Median sternotomy approach for coronary artery bypass grafting or heart valvereplacement procedures.
Exclusion
Exclusion Criteria:
- With a history of benzodiazepine allergy
- Significant liver or kidney insufficiency
- Coagulation dysfunction
- Neurological or psychiatric disorders
- Undergone major surgery within the past three months.
Study Design
Total Participants: 80
Treatment Group(s): 2
Primary Treatment: Propofol injection
Phase:
Study Start date:
August 01, 2022
Estimated Completion Date:
September 01, 2023
Connect with a study center
Shanghai East Hospital of Tongji University
Shanghai, Shanghai 200120
ChinaActive - Recruiting

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