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Clinical application study of propofol combined with alfentanil anesthesia in tumor interventional surgery

Clinical application study of propofol combined with alfentanil anesthesia in tumor interventional surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104450
Enrollment
Unknown
Registered
2025-06-17
Start date
2025-06-20
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Interventional therapy for tumors

Interventions

Intervention group:Cyclopofol+Alfentanil
ci-Profol:Propofol+Alfentanil

Sponsors

Lishui Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients who intend to undergo tumor interventional therapy; 2. Age> = 18 years old, gender is not limited; 3. ASA is graded as Grade II~III.; 4.18Kg/m^2<=BMI<=25kg/m^2; 5. Clearly understand and voluntarily participate in the study, and sign the informed consent form by themselves or their family members.

Exclusion criteria

Exclusion criteria: 1. Patients with severe respiratory insufficiency, obstructive pulmonary disease, history of bronchospasm requiring treatment in the past 3 months, acute respiratory infection within 1 week, and obvious symptoms such as fever, wheezing, nasal congestion and cough; Proposed endotracheal intubation for general anesthesia; 2. Have serious heart diseases such as severe arrhythmia, heart failure, unstable angina, severe myocardial infarction in the past 6 months, severe heart valve disease, etc.; 3. History of severe cerebrovascular disease and epilepsy; 4. Patients with severe liver and kidney dysfunction; 5. Patients who are allergic to propofol or cyclopofol; 6. People with communication difficulties such as schizophrenia and intellectual disability; 7. Other conditions judged by the investigator to be unsuitable for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
The incidence rate of adverse events related to the respiratory system (respiratory depression, apnea, hypoxia);

Secondary

MeasureTime frame
Research drug use;Evaluation of cyclopofol compared with propofol in tumor interventional therapy: Hypotension requiring intervention (SBP <) 90mmHg or a 30% decrease from the baseline with a duration of more than 2 m;Duration of full consciousness ;The occurrence and severity of nausea and vomiting;Sedation/anesthesia satisfaction evaluation;Safety evaluation;

Countries

China

Contacts

Public ContactHao Cheng

Lishui Central Hospital

332319747@qq.com+86 579 83831085

Outcome results

None listed

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