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Effect of sequential use of remazolam besylate on extubation time in mechanically ventilated ICU patients

Effect of sequential use of remazolam besylate on extubation time in mechanically ventilated ICU patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065048
Enrollment
Unknown
Registered
2022-10-26
Start date
2022-10-30
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Patients requiring mechanical ventilation in the ICU

Interventions

remimazolam besylate:The sedative drug was changed to remimazolam benzenesulfate 12 hours before SBT test: loading dose 0.2mg/kg, maintenance dose 0.1-1.0mg/kg/h
Conrol group:12 hours before SBT test, sedatives were converted to:Midazolam loading dose 0.03-0.3mg/kg, maintenance dose 0.04-0.2mg/kg/h

Sponsors

Xijing hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)age;18-80 years 2) First admission to ICU; 3) Intubated patients who are expected to receive mechanical ventilation for =24 hours in the ICU; 4) Informed consent was obtained from patients or family members.18-80

Exclusion criteria

Exclusion criteria: 1. known or suspected allergy to the test drug ; 2. pregnant and lactating women ; 3. Severe obesity ( BMI >= 35 kg/m2 ) ; 4. Chronic liver and kidney dysfunction: chronic liver failure: Child-pugh improved classification of 10-15 points ( C grade ); chronic renal failure: KDIGO diagnostic criteria >=CDK3 [stage 4 [ GFR or eGFR 15-29 mL/( min 1.73m2 )] and stage 5 [ GFR or eGFR < 15 mL/( min 1.73m2 )], eGFR was calculated using the modification of diet in renal disease study ( MDRD ) formula: eGFR = 170*serum creatinine (SCr) -1.234*age -0.179*0.79 (female)] 5. history of alcoholism or taking anti-anxiety drugs or hypnotics ; 6. Patients with expected difficulty in weaning ( such as high spinal cord injury or advanced amyotrophic lateral sclerosis ) ; 7. Coma due to craniocerebral trauma, status epilepticus and unknown etiology ; 8. patients who stopped treatment due to poor prognosis ; 9. Patients who participated in other studies within 3 months.

Design outcomes

Primary

MeasureTime frame
Time from cessation of sedation administration to extubation;

Countries

china

Contacts

Public Contactzhangxijing

Xijing hospital

zhangxj918@163.com13384920881

Outcome results

None listed

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