Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06531915

Comparison of Efficacy and Safety Between Ciprofol and Remimazolam During Fiberoptic Bronchoscopy

Comparison of Efficacy and Safety Between Ciprofol and Remimazolam During Fiberoptic Bronchoscopy: a Study Protocol for a Single-center, Double-blind, Randomized Controlled Trial

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
190 (estimated)
Sponsor
Anhui Provincial Hospital · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Both ciprofol and remimazolam have been found to be potential alternatives to propofol (a commonly used anesthesia) during fiberoptic bronchoscopy, while the efficacy and safety between ciprofol and remimazolam have not been reported. This study aims to compare the efficacy and safety between ciprofol and remimazolam in patients undergoing fiberoptic bronchoscopy.

Conditions

Interventions

TypeNameDescription
DRUGCiprofolParticipants in the ciprofol group will be intravenously injected with 0.4 mg/kg of ciprofol (batch number H20200013, Haisike Pharmaceutical Co., Ltd., Liaoning, China) and sufentanil (0.2 μg/kg).
DRUGRemimazolamParticipants in the remimazolam group will be intravenously injected with 0.1 mg/kg of remimazolam besylate (batch number HR7056, Hengrui Pharmaceutical Co., Ltd., Jiangsu, China) and sufentanil (0.2 μg/kg).

Timeline

Start date
2024-12-01
Primary completion
2024-12-30
Completion
2025-03-31
First posted
2024-08-01
Last updated
2024-08-01

Source: ClinicalTrials.gov record NCT06531915. Inclusion in this directory is not an endorsement.