Geneva, Sept. 21 -- International Clinical Trials Registry received information related to the study (NCT07805876) titled 'The Effect of Ciprofol Versus Propofol Anesthesia on Postoperative Neurological Complications' on Sept. 1.
Study Type: Interventional
Study Design:
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Prevention. Masking: Double (Participant, Outcomes Assessor).
Primary Sponsor: Beijing Tiantan Hospital
Condition:
Intracranial Tumors
Intervention:
Drug: Ciprofo
Recruitment Status: Not recruiting
Phase: N/A
Date of First Enrollment: September 7, 2026
Target Sample Size: 434
Countries of Recruitment:
China
To know more, visit https://clinicaltrials.gov/study/NCT07805876
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