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To investigate the clinical application of remimazolam for patient-controlled sedation (PCS)

To investigate the clinical application of remimazolam for patient-controlled sedation (PCS)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099212
Enrollment
Unknown
Registered
2025-03-19
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

operative complications

Interventions

Remazolam group:Sedation was induced by remimazolam
Control group:Sedation was induced by propofol

Sponsors

The First Affiliated Hospital, Medical School of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: This project will be applied to patients undergoing endoscopic cholangiopancreatography (ERCP). Inclusion criteria: 1. Age >18 years old; 2. Patients and their families signed the informed consent; 3. ASA grade I-III; 4. patients who understand and correctly use PCS equipment.

Exclusion criteria

Exclusion criteria: 1. Patients allergic to remimazolam tosilate used in PCS; 2. The patient had severe cardiopulmonary dysfunction and could not tolerate the physiological changes caused by sedative drugs; 3. Patients had severe coagulopathy or bleeding tendency, which may increase the risk during sedation; 4. patients with severe central nervous system history or sedative drug abuse history; 5. patients with difficult tracheal intubation, patients with severe sleep apnea syndrome or other sleep disorders.

Design outcomes

Primary

MeasureTime frame
The number of patients who reached an appropriate state of sedation (Ramsay score 2-4) within 5 minutes;

Secondary

MeasureTime frame
Bispectral index;blood pressure;SPO2;

Countries

China

Contacts

Public ContactZhu Yaomin

The First Affiliated Hospital, Medical School of Xi'an Jiaotong University

yaomin_zhu@126.com+86 186 2938 2846

Outcome results

None listed

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