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Comparison of anterograde amnesia effects of different doses of remimazolam: A prospective randomized controlled single-blind clinical study

Comparison of anterograde amnesia effects of different doses of remimazolam: A prospective randomized controlled single-blind clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095205
Enrollment
Unknown
Registered
2025-01-03
Start date
2025-02-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Anterograde amnesia

Interventions

Control group:NS infusion
Low dosage remimazolam group:0.075mg/kg induction+infusion
high dosage remimazolam group:0.15mg/kg induction+infusion

Sponsors

Shenzhen University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1Age 18~65 years; 2BMI 18~28kg/m2; 3ASA I~III; 4Without obstructive sleep apnea syndrome; 5Selective operation with spinal anesthesia or nerve block anesthesia and operation duration>60min; 6sign the informed consent

Exclusion criteria

Exclusion criteria: 1Interventional surgery; 2breath difficult; 3mental disorders, cognitive dysfunction or serious systemic diseases; 4undergoing general anesthesia within 7 days before inclusion of the study; 5allergic to benzodiazepines, opioids, or other pharmaceutical ingredients; 6spinal anesthesia or nerve block anesthesia with difficults, unexpected long time and imperfect anesthesia effects

Design outcomes

Primary

MeasureTime frame
Anterograde amnesia degree;(QoR-15) score;

Secondary

MeasureTime frame
life signs;BIS;MOAA/S score;Complications;

Countries

China

Contacts

Public ContactJun Xiong

Shenzhen University General Hospital, Shenzhen University

xiongjun107@hotmail.com+86 138 1019 7854

Outcome results

None listed

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