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Clinical study of remazolam toluenesulfonate for fiberoptic bronchoscopy and treatment

Clinical study of remazolam toluenesulfonate for fiberoptic bronchoscopy and treatment

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045543
Enrollment
Unknown
Registered
2021-04-19
Start date
2021-05-01
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

Respiratory disease

Interventions

Experimental group:Sequential method

Sponsors

Hainan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients who intend to be examined and treated by fiberoptic bronchoscopy; 2.At the ASA I~II level; 3.The age is 18 to 65 years old; 4.The patient signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Obesity (body mass index > 30kg/m^2); 2.Patients with recent bronchial asthma or massive hemoptysis; 3.patients with severe stenosis of the main airway; 4.Patients with myasthenia gravis; 5.Patients with schizophrenia; 6.Patients with severe depression or with a long history of benzodiazepine use; 7.Patients who are scheduled to be examined/ treated with fiberoptic bronchoscopy for more than 30 minutes.

Design outcomes

Primary

MeasureTime frame
Incidence of serious adverse events;Incidence of solicited adverse events;Incidence of unsolicited adverse events;

Countries

China

Contacts

Public ContactJia Zhen

Hainan Cancer Hospital

ggfun@163.com+86 18638689770

Outcome results

None listed

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