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Sedative Efficacy of Remimazolam Besylate for Fiberoptic Bronchoscopy and Treatment in Non-Intubated ICU Patients and Its Impact on Hemodynamic Parameters — A Prospective, Observational Clinical Study

Sedative Efficacy of Remimazolam Besylate for Fiberoptic Bronchoscopy and Treatment in Non-Intubated ICU Patients and Its Impact on Hemodynamic Parameters — A Prospective, Observational Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123216
Enrollment
Unknown
Registered
2026-04-22
Start date
2026-04-27
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Respiratory Diseases

Interventions

Observation group(Remimazolam Besylate):None

Sponsors

Chengdu Third People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.The subject is ineligible for trial participation if they do NOT meet ALL of the following criteria: (1) Aged 18 years or older, regardless of gender; (2) Non-intubated patients in the ICU requiring fiberoptic bronchoscopy; (3) The patient or their legal guardian voluntarily agrees to participate in this study and provides signed informed consent.

Exclusion criteria

Exclusion criteria: 1.The subject is ineligible for trial participation if ANY of the following criteria applies: (1) Allergy to remimazolam besylate or any component of the investigational or concomitant medications; (2) Severe circulatory instability (e.g., MAP 20 mmHg) or status epilepticus; (4) Pregnancy or lactation; (5) Electrocardiogram indicating a heart rate < 50 beats per minute; (6) History of alcohol or drug abuse, or chronic pain requiring long-term use of analgesics or sedatives; (7) History of severe hepatic or renal dysfunction, metabolic diseases, or related conditions; (8) Participation in any other investigational clinical trial within 3 months prior to screening; (9) Expected survival time < 48 hours. (10) Inability to obtain informed consent or authorization; (11) Other conditions considered by the investigators to be not included in the study.

Design outcomes

Primary

MeasureTime frame
RASS score;

Countries

China

Contacts

Public ContactZeng Wei

Chengdu Third People's Hospital

456zw@163.com+86 159 0288 8821

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026