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A study on the effectiveness and safety of remimazolam fast-track anesthesia in interventional surgery in patients with heart disease

A study on the effectiveness and safety of remimazolam fast-track anesthesia in interventional surgery in patients with heart disease

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109737
Enrollment
Unknown
Registered
2025-09-24
Start date
2024-01-09
Completion date
Unknown
Last updated
2025-09-29

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

Conditions

heart disease

Interventions

Remazolam group (Age 2-8):Remimazolam 0.3 mg·kg-1 for anesthesia induction and 1 mg·kg-1·h-1 for maintenance
Propofol group (Age 2-8):Propofol was used for induction of anesthesia at 3 mg·kg-1 and 8 mg·kg-1·h-1 for maintenance.
Remazolam group (Age 65-80):Remimazolam 0.3 mg·kg-1 for anesthesia induction and 1 mg·kg-1·h-1 for maintenance
Propofol group (Age 65-80):Propofol was used for induction of anesthesia at 3 mg·kg-1 and 8 mg·kg-1·h-1 for maintenance.

Sponsors

Central China Fu Wai Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Age 2-8 years; 2) Children who are scheduled to undergo interventional surgery for congenital heart disease under general fast-track anesthesia; 3) Age 65-80 years; 4) Elderly patients who are scheduled to undergo interventional surgery for congenital heart disease under general fast-track anesthesia; 5) Voluntarily signed the informed consent form.

Exclusion criteria

Exclusion criteria: Exclusion Criteria: 1) Children with cyanotic complex congenital heart disease; 2) Combined with other congenital diseases; 3) Patients who have previously undergone intracardiac intervention or surgical recurrence and need interventional treatment again; 4) Patients with communication disorders, including language and hearing disorders, and those unable to understand Mandarin; 5) Patients who are allergic or may be allergic to the study drug; 6) Participation in other clinical investigators within 3 months.

Design outcomes

Primary

MeasureTime frame
Time to extubation;Time of loss of consciousness;Number of sedation failures, etc.;

Secondary

MeasureTime frame
Postoperative consciousness score;Hospitalization days;

Countries

China

Contacts

Public ContactPengyu Qin

Henan Provincial People’s Hospital, Department of Anesthesia of central China Fu Wai Hospital of Zhengzhou University

1061407570@qq.com+86 189 3722 9723

Outcome results

None listed

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