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The application of low-dose esketamine combined with cyclopofol in endoscopic retrograde cholangiopancreatography in elderly patients

The application of low-dose esketamine combined with cyclopofol in endoscopic retrograde cholangiopancreatography in elderly patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107838
Enrollment
Unknown
Registered
2025-08-19
Start date
2025-08-19
Completion date
Unknown
Last updated
2025-08-25

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

Conditions

Diseases of the biliary tract and pancreas

Interventions

Experimental Group:Low-dose esketamine combined with cyclopofol group
Control group:Sufentanil combined with propofol group

Sponsors

Quzhou People Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 65 and 80; 2.) The anesthesia risk classification of the American Academy of Anesthesiologists (ASA) is grade II to III; 3. Body mass index (BMI) : 18 to 30 kg/m^2; 4. To undergo endoscopic retrograde cholangiopancreatography (ERCP) at an elective date; 5. Be able to understand the research content and voluntarily sign a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those who are allergic to the test drugs (esketamine, cyclopofol, sufentanil or propofol); 2. Has a history of severe hypertension, intracranial hypertension, uncontrolled hyperthyroidism, or glaucoma; 3. Those who have had respiratory tract infections or significantly impaired lung function recently; 4. Has a history of severe craniocerebral trauma or cerebrovascular accident in the past; 5. Those with mental disorders or who have been taking antipsychotic drugs for a long time; 6. Those with severe liver or kidney dysfunction, ascites or renal failure; 7. Patients with severe sleep apnea syndrome; 8. Failing to sign the informed consent form or refusing to participate in this researcher;

Design outcomes

Primary

MeasureTime frame
During the operation, vital signs (HR, MAP, SPO?) indicators at key time points were continuously recorded;

Countries

China

Contacts

Public ContactShufen Yang

Quzhou People Hospital

yangsf123@sina.cn+86 13575647461

Outcome results

None listed

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