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Half effective dose of remimazolam for loss of consciousness in patients of different ages

Half effective dose of remimazolam for loss of consciousness in patients of different ages

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066581
Enrollment
Unknown
Registered
2022-12-09
Start date
2022-12-15
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

Induction of general anesthesia

Interventions

Group A(18-29 years):Remazolam 0.2mg/kg intravenously
Group B(30-39 years): Remazolam 0.2mg/kg intravenously
Group C(40-49 years): Remazolam 0.2mg/kg intravenously
Group D(50-59 yaers):Remazolam 0.2mg/kg intravenously
Group E(60-69 years):Remazolam 0.16mg/kg intravenously
Group F(70-79 years):Remazolam 0.10mg/kg intravenously
Group G(>80 years):Remazolam 0.10mg/kg intravenously

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adults with normal mental and physical development,ASA grade ?-?, who needed to undergo examination/surgery due to their condition in the day surgery center and operating room of our hospital were selected.

Exclusion criteria

Exclusion criteria: Age < 18 years; Allergic to benzodiazepines and any ingredient of this product; Mental health problems; Severe respiratory diseases; Serious cardiovascular diseases; Severe liver and kidney dysfunction; Patients with myasthenia gravis.

Design outcomes

Primary

MeasureTime frame
Half effective dose of rimazolam for loss of consciousness in patients of different ages;Loss of consciousness (MOAA/S score =1 within 3 minutes after intravenous remazolam);Incidence of adverse reactions: injection pain, hiccup, body movement, increased speech, muscle fibrillation, respiratory depression (SPO2<90%, RR<10 times/min), cough, awareness;

Secondary

MeasureTime frame
The induction dose;BIS score;Give remazolam until you lose consciousness;After entering the operating room, the baseline value (T0) and the administration of remazolam were Carve RR, SpO?, HR, and MAP for (T1), 1min(T2), 2min(T3), and 3min (T4).;

Countries

China

Contacts

Public ContactYunan Lin

The First Affiliated Hospital of Guangxi Medical University

277464077@qq.com13768278751

Outcome results

None listed

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