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Effect of remimazolam tosilate versus propofol during drug-induced sleep endoscopy in patients with obstructive sleep apnea hypopnea syndrome

Effect of remimazolam tosilate versus propofol during drug-induced sleep endoscopy in patients with obstructive sleep apnea hypopnea syndrome

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053973
Enrollment
Unknown
Registered
2021-12-04
Start date
2021-12-01
Completion date
Unknown
Last updated
2022-11-07

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

Conditions

Obstructive sleep apnea hypopnea syndrome

Interventions

Experimental group:Intravenous remimazolam tosilate (0.2 mg/kg) before examination

Sponsors

Xiangya Hospital of Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with obstructive sleep apnea hypopnea syndrome before surgery and planning to undergo drug-induced sleep endoscopy; 2. Aged 18 to 60 years; 3. ASA is graded I-III.

Exclusion criteria

Exclusion criteria: 1. Those who intend to receive endotracheal intubation or implantation of a laryngeal mask; 2. Patients who have recently used sedatives or analgesics; 3. Those who are allergic or contraindicated to benzodiazepines, opioids, propofol and their components; 4. Patients with severe respiratory and circulatory insufficiency; 5. People with mental illness, long-term use of psychotropic drugs and cognitive impairment; 6. Patients with severe immune insufficiency (such as AIDS, etc.); 7. Patients with severe hepatic and renal insufficiency; 8. Pregnant or lactating patients; 9. Those who have participated in other clinical trials within the last 3 months.

Design outcomes

Primary

MeasureTime frame
Sedation success rate;Heart rate;non-invasive blood pressure;

Countries

China

Contacts

Public ContactHuang Changsheng

Xiangya Hospital of Central South University

changsheng.huang@csu.edu.cn+86 15974172150

Outcome results

None listed

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