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A randomized controlled trial of oliceridine combined with propofol in painless endoscopic injection sclerotherapy for cirrhotic patients in China

A randomized controlled trial of oliceridine combined with propofol in painless endoscopic injection sclerotherapy for cirrhotic patients in China

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121052
Enrollment
Unknown
Registered
2026-03-24
Start date
2025-04-02
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

painless endoscopic injection sclerotherapy for cirrhotic patients in China

Interventions

oliceridine group:The patients in the oliceridine group were given a dose of 0.03 mg/kg oliceridine
sufentanil group: The patients in the sufentanil group were given a dose of0.15 µg/kg sufentanil

Sponsors

Beijing You'an Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients with cirrhosis of various etiologies; 2.American Society of Anesthesiologists (ASA) physical status ?–?; 3. Aged 18–65 years, regardless of gender; 4. Liver function classified as Child-Pugh grade A or B; 5. Meeting the indications for painless EIS; 6.Patients who agreed to undergo sedated or anesthetized gastroscopy and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Non-cirrhotic patients; 2. Patients with contraindications to conventional gastroscopy; 3. Patients who refused sedation or anesthesia for gastroscopy; 4. Patients allergic to components of sedatives or anesthetics; 5. Patients unable to complete the questionnaire due to various reasons.

Design outcomes

Primary

MeasureTime frame
Intraoperative respiratory depression;

Secondary

MeasureTime frame
Vital signs including SBP, DBP, MAP, HR, RR, and SpO?;Incidence of adverse reactions: including specific adverse reactions (nausea, vomiting, dizziness, fever, and drowsiness) and other non-specific adverse reactions.;Anesthesia satisfaction of patients and gastroscopists;

Countries

China

Contacts

Public ContactGuan Lei

Beijing You'an Hospital, Capital Medical University

Willqun1@sina.com+86 10 8399 7160

Outcome results

None listed

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