Clinical Trials Directory

Trials / Unknown

UnknownNCT05971121

Comparing Ciprofol and Propofol for Sedation in Hypotensive ICU Patients: a Single Center Prospective Cohort Study

Status
Unknown
Phase
Study type
Observational
Enrollment
456 (estimated)
Sponsor
Nanfang Hospital, Southern Medical University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study was a single-center, prospective, 2-year observational cohort study. The study subjects were ICU patients requiring vasopressor drugs and requiring sedation. According to the use of ciprofol or propofol in the treatment plan (determined by the doctor in charge according to the condition of the subjects), they were divided into groups: ciprofol group and propofol group. A total of 456 subjects were planned to be enrolled, including 304 subjects in the cyclopofol group and 152 subjects in the propofol group. The data of this study were obtained by extracting the routine clinical diagnosis and treatment records of the enrolled subjects.

Conditions

Interventions

TypeNameDescription
DRUGciprofolCiprofol were used for sedation in ICU hypotensive patients

Timeline

Start date
2022-10-01
Primary completion
2024-10-01
Completion
2024-10-01
First posted
2023-08-02
Last updated
2023-08-02

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05971121. Inclusion in this directory is not an endorsement.