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ED50 and ED90 of remimazolam for total intravenous anesthesia combined with intranasal dexmedetomidine in pediatric MRI

ED50 and ED90 of remimazolam for total intravenous anesthesia combined with intranasal dexmedetomidine in pediatric MRI

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081218
Enrollment
Unknown
Registered
2024-02-26
Start date
2024-03-01
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

none

Interventions

3-6 age group:30 minutes before MRI examination, dexmedetomidine (3 µg/kg) was given intranasally. Remimazolam was then given intravenously before MRI examination. The dose of remimazolam was determin
1-3 age group:30 minutes before MRI examination, dexmedetomidine (3 µg/kg) was given intranasally. Remimazolam was then given intravenously before MRI examination. The dose of remimazolam was determin
3 month-1 age group:30 minutes before MRI examination, dexmedetomidine (3 µg/kg) was given intranasally. Remimazolam was then given intravenously before MRI examination. The dose of remimazolam was de

Sponsors

Guangzhou Women and Children’s Medical Center, Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0.3 Years to 6 Years

Inclusion criteria

Inclusion criteria: The hospitalized children who required sedation during magnetic resonance imaging (MRI) were enrolled. The examination time was expected to be less than 1 hour, and the age between 3 months and 6 years old with an American Standards Association physical status of I–III.

Exclusion criteria

Exclusion criteria: History of anaphylaxis to anesthetics, unstable vital signs, severe heart and lung diseases, severe liver and kidney dysfunction, upper respiratory tract infection, severe sleep apnea syndrome or other airway obstructive diseases, use of sedatives within 48 hours before examination.

Design outcomes

Primary

MeasureTime frame
sedation results of remimazolam;dose of remimazolam;

Secondary

MeasureTime frame
Use of rescue sedation drugs during induction;Use of sedation drugs during examination;Blood pressure;Heart rate;Oxygen saturation;

Countries

China

Contacts

Public ContactWanjun Zheng

Guangzhou Women and Children’s Medical Center, Guangzhou Medical University

77729381@qq.com+86 136 4508 0867

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 22, 2026