Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07294989

The Effective Blood Concentration of Ciprofol

Median Effective Concentration of Ciprofol and Its Correlation With Bispectral Index: A Prospective Observational Study

Status
Recruiting
Phase
Study type
Observational
Enrollment
101 (estimated)
Sponsor
Peking University Shenzhen Hospital · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

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

Interventions

TypeNameDescription
DRUGCiprofolBeginning with an initial target plasma concentration of ciprofol at 1.2 μg/mL. Assessments of the Modified Observer's Assessment of Alertness/Sedation (MOAA/S) scale and Bispectral Index (BIS) values are performed every minute until the patient achieves a complete anesthetic state (defined as an MOAA/S score of 0).

Timeline

Start date
2025-07-01
Primary completion
2026-06-30
Completion
2026-06-30
First posted
2025-12-19
Last updated
2026-01-06

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07294989. Inclusion in this directory is not an endorsement.