Actively Recruiting
The Effective Blood Concentration of Ciprofol
Led by Peking University Shenzhen Hospital · Updated on 2026-01-06
101
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
1. Eligible patients were selected and enrolled in the study. 2. General anesthesia was induced using ciprofol in all participants, with standardized evaluation of consciousness levels during induction. 3. The patients' pain and cognition are followed up after surgery.
CONDITIONS
Official Title
The Effective Blood Concentration of Ciprofol
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18-65 years
- Scheduled for elective thyroidectomy
- ASA physical status classification I-II
- Willing to participate and providing written informed consent
You will not qualify if you...
- Recent use of sedatives or opioid analgesics
- Severe hepatic or renal dysfunction defined as: Child-Pugh class C (score 6510), Creatinine clearance <35 mL/min, Requiring preoperative dialysis
- Significant cardiovascular comorbidities
- Body mass index 6535 kg/m5B2 or <18.5 kg/m5B2
- Known hypersensitivity or adverse reactions to propofol/ciprofol
- Neuropsychiatric disorders including: Alzheimer's disease, History of cerebrovascular events, Traumatic brain injury, Space-occupying brain lesions, Other significant neurological deficits
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Peking University Shenzhen Hospital
Shenzhen, Guangdong, China
Actively Recruiting
Research Team
T
Tao Luo
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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