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A study of remimazolam on sedation in elderly patients with mechanical ventilation

A study of remimazolam on sedation in elderly patients with mechanical ventilation

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078823
Enrollment
Unknown
Registered
2023-12-19
Start date
2022-07-01
Completion date
Unknown
Last updated
2024-01-14

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

Conditions

elderly patients with mechanical ventilation

Interventions

Sponsors

The First Aftiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 85 Years

Inclusion criteria

Inclusion criteria: ? Aged from 65 years old to 85 years old ? Patients with mechanical ventilation ? Sign an informed consent form

Exclusion criteria

Exclusion criteria: ? Pregnancy or breastfeeding ? Severe pre-existing parenchymal liver disease with clinically significant portal hypertension Child-Pugh grade C cirrhosis or acute liver failure ? Severe head injury Brain tumor increased intracranial pressure increased cerebrovascular accidental coma, status epilepticus, etc. ? Patients with a history of alcohol or substance abuse ? Patients requiring deep sedation (RASS<-2) depending on the clinical consideration of the condition ? Severe arrhythmias (eg, third-degree AV block with no pacemaker sinus bradycardia<50 beats/min) ? Patients with allergies to remazolam benzodiazepines ? Patients who are unable to obtain informed consent ? He is participating in other relevant clinical drug validation studies

Design outcomes

Primary

MeasureTime frame
Sedation compliance rate;

Secondary

MeasureTime frame
Sedation onset time;Wake-up time after deactivation;Mechanical ventilation time;Length of ICU hospital stay;Incidence of delirium;Incidence of adverse reactions;

Countries

China

Contacts

Public ContactJun Wang

The First Aftiliated Hospital of Soochow University

dr_wangjun@suda.edu.cn+86 186 0627 8680

Outcome results

None listed

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