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The safety and efficacy of different doses of esketamine combined with remimazolam for anesthesia in patients undergoing ERCP

The safety and efficacy of different doses of esketamine combined with remimazolam for anesthesia in patients undergoing ERCP

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083267
Enrollment
Unknown
Registered
2024-04-19
Start date
2024-04-22
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

Anesthesia for patients undergoing ERCP surgery

Interventions

Low-dose esketamine group:Anesthesia induction (esketamine 0.25 mg/kg + remimazolam 0.2 mg/kg) + anesthesia maintenance (esketamine 0.5 mg/kg/h + remimazolam 1 mg/kg/h)
High-dose esketamine group:Anesthesia induction (esketamine 0.4 mg/kg + remimazolam 0.2 mg/kg) + anesthesia maintenance (esketamine 0.5 mg/kg/h + remimazolam 1 mg/kg/h)
Propofol combined with remifentanil group:Anesthesia induction (propofol 1.5 mg/kg + remifentanil 1 ug/kg) + anesthesia maintenance (propofol 5 mg/kg/h + remifentanil 5 ug/kg/h)

Sponsors

The Affiliated Hospital of Guizhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Age: 18~75 years old; (2)BMI:18~30(kg/m2); (3) ASA classification: I~III; (4) Patients who have been excluded from contraindication to surgery and intend to undergo ERCP; (5) Patients who intend to participate in the trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Hearing or vision impairment and inability to cooperate; (2) Allergy to the known drugs involved in the use or contraindication of use; (3) the presence of psychiatric diseases; (4) poorly controlled hypertension; (5) Those with severe coronary heart disease or heart failure and cardiac function is grade III~IV; (6) Combined with other systemic serious diseases: such as abnormal coagulation function, liver and kidney dysfunction, etc.

Design outcomes

Primary

MeasureTime frame
Incidence of hypoxemia;Modified alertness/sedation score;

Secondary

MeasureTime frame
Incidence of hypotension;Movement occurs;Degree of choking reaction;

Countries

China

Contacts

Public ContactOu Wei

The Affiliated Hospital of Guizhou Medical University

425719659@qq.com+86 136 3908 7981

Outcome results

None listed

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