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Effect of Remazolam besylate and propofol on the incidence of sedation adverse events in patients treated with painless bronchoscopy

Effect of Remazolam besylate and propofol on the incidence of sedation adverse events in patients treated with painless bronchoscopy

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500099355
Enrollment
Unknown
Registered
2025-03-21
Start date
2025-03-30
Completion date
Unknown
Last updated
2025-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diseases requiring painless bronchoscopy

Interventions

Remazolam benzosulfonate Group (Group A):None
Propofol group (Group B):None
Remazolam benzosulfonate combined with Propofol group (Group C):None

Sponsors

Chongqing Public health medical treatment Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients selected for painless fiberoptic treatment in our hospital; 2. age > 18 years old, male or female; 3. The patient voluntarily signs a written informed consent; 4. American Society of Anesthesiologists Grade I-III.

Exclusion criteria

Exclusion criteria: 1. Patients who are known to be allergic to any of the drug components intended for use or who have contraindications to any of the medications; 2. Patients with long-term use of benzodiazepines; 3. Patients with severe renal dysfunction (requiring kidney replacement therapy); 4. Patients who are participating in any interventional clinical trial; 5. Individuals with hearing, intellectual, communication, or cognitive impairments 6.Patients who, for any reason, are unable to cooperate with the study or are deemed by the investigator to be unsuitable for participation in this research.

Design outcomes

Primary

MeasureTime frame
Pulse Oxygen Saturation;Feasibility of diagnosis and treatment procedures (vocal cord movement, coughing, body movement);Non-invasive blood pressure;

Secondary

MeasureTime frame
Pain at the injection site;Patient's intention to review;

Countries

China

Contacts

Public ContactRongdanTan

Chongqing Public health medical treatment Center

wlq507cqmu@163.com+86 134 5245 3321

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026