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The Effect of Oliceridine Infusion on Hemodynamics During ERCP: A Randomized Clinical Trial

The Effect of Oliceridine Infusion on Hemodynamics During ERCP: A Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110017
Enrollment
Unknown
Registered
2025-09-28
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

ERCP

Interventions

Oliceridine group:All patients were placed in a semi-prone position (right side elevated by 30 degrees). Patients in the oliceridine group received intravenous administration of 0.4 mg/kg esketamine,
Control group:The control group received intravenous 0.4 mg/kg esketamine, 2 ml saline, and 0.2–0.4 mg/kg remifentanil, and all patients were maintained on 1–1.25 mg/kg/h remifentanil by infusion.

Sponsors

Shanghai East Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients scheduled for endoscopic retrograde cholangiopancreatography (ERCP), aged >=65 years, with an American Society of Anesthesiologists (ASA) physical status classification of III–IV.

Exclusion criteria

Exclusion criteria: 1. Patients with history of mental illness, using antipsychotic drugs 2. Patients with allergies or contraindications to Cyclopropane, Esketamine, Oliceridine, and soybeans 3. Patients with severe risk of elevated blood pressure or intracranial pressure; poorly controlled or untreated hypertensive patients 4. Patients with severe hepatic and renal functional decompensation 5. Abnormal electrocardiogram: including corrected QT interval greater than 450 milliseconds.

Design outcomes

Primary

MeasureTime frame
Hypoxia-related adverse events occurring during sedation;

Countries

China

Contacts

Public ContactLu Xinge

Tongji University School of Medicine,Shanghai East Hospital

luxinge95@163.com+86 131 9044 4310

Outcome results

None listed

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