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To compare the efficacy and safety of remimazolam and dexmedetomidine intravenous sedation in children with magnetic resonance imaging

To compare the efficacy and safety of remimazolam and dexmedetomidine intravenous sedation in children with magnetic resonance imaging

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077381
Enrollment
Unknown
Registered
2023-11-07
Start date
2023-11-10
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Magnetic resonance imaging was performed in children

Interventions

Dexmedetomidine group:Sedative drug is dexmedetomidine

Sponsors

Kunming Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 10 Years

Inclusion criteria

Inclusion criteria: (1) outpatients or inpatients scheduled for MRI examination; (2) age 1-10 years old; (3) ASA grade I-II; (4) voluntarily participate in and sign the informed consent

Exclusion criteria

Exclusion criteria: (1) children with known hemodynamic or respiratory instability, airway abnormalities, cardiac defects or arrhythmias; (2) known to be allergic to remimazolam besylate and dexmedetomidine; (3) current use of dexmedetomidine or benzodiazepines for any treatment; (4) patients with cognitive impairment; (5) researchers considered that they were not suitable to participate in the clinical trial for other reasons.

Design outcomes

Primary

MeasureTime frame
Time of recovery;

Secondary

MeasureTime frame
Time to onset;Heart rate;Blood pressure;Scan time;Whether to take remedial action;Whether flumazenil is needed;Adverse event rate;

Countries

China

Contacts

Public ContactLi Guoyan

Kunming Children's Hospital

guoyanli94@163.com+86 183 1386 6814

Outcome results

None listed

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