Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT07294989

The Effective Blood Concentration of Ciprofol

Sponsor: Peking University Shenzhen Hospital

View on ClinicalTrials.gov

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.

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

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

OBSERVATIONAL

Enrollment

101

Start Date

2025-07-01

Completion Date

2026-06-30

Last Updated

2026-01-06

Healthy Volunteers

No

Conditions

Interventions

DRUG

Ciprofol

Beginning 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).

Locations (1)

Peking University Shenzhen Hospital

Shenzhen, Guangdong, China