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
| Type | Name | Description |
|---|---|---|
| DRUG | ciprofol | Ciprofol 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.