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The efficacy and safety of Oliceridine in fiberoptic bronchoscopy for elderly patients

The efficacy and safety of Oliceridine in fiberoptic bronchoscopy for elderly patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116232
Enrollment
Unknown
Registered
2026-01-07
Start date
2026-01-19
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

pulmonary disease

Interventions

Experimental Group (Group O):Oliceridine:Oxalidine 0.02mg/kg was administered followed by remimazolam 0.3 mg/kg
Control group (Group S) :sufentanil :Sufentanil 0.1ug/kg was administered followed by remimazolam 0.3 mg/kg

Sponsors

Qiannan People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Painless fiberoptic bronchoscopy is planned to be performed; 2. Patients of any gender, aged 65 to 80, who can understand and sign the informed consent form; 3.ASA classification grades I - III; 4. No cognitive impairment, mental abnormality or communication disorder; 5. No participation in other clinical studies was conducted within the three months prior to inclusion.

Exclusion criteria

Exclusion criteria: 1.Severe liver and kidney dysfunction, hemostatic dysfunction, and satiety or gastrointestinal obstruction accompanied by retention of gastric contents; 2. Uncontrolled and potentially life-threatening circulatory and respiratory diseases (such as acute coronary syndrome, uncontrolled severe hypertension, severe arrhythmia, severe heart failure, recently occurred acute myocardial infarction, and acute asthma attacks, etc.); 3. Patients with mental abnormalities who are unable to understand the relevant content informed; 4. Those with severe difficult airways (Modified Markov Scale grade IV); 5. Those who are allergic to or have contraindications to the drugs used in this research.

Design outcomes

Primary

MeasureTime frame
Cough and body movement score;

Secondary

MeasureTime frame
HR,MAP,SPO2;Increase the dosage of sedatives;The number of endoscopic interruptions;Postoperative QoR-15 scale score;The frequency of pressurized oxygen supply;standing time of PACU;Adverse events (dizziness, nausea, vomiting, etc.);

Countries

China

Contacts

Public ContactKuiquan Ji

Qiannan People's Hospital

jikq@163.com+86 186 8508 9061

Outcome results

None listed

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