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A Study on the Efficacy of Oliceridine Combined with Propofol in Painless Bronchoscopy

A Study on the Efficacy of Oliceridine Combined with Propofol in Painless Bronchoscopy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123221
Enrollment
Unknown
Registered
2026-04-22
Start date
2026-04-30
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Bronchial diseases

Interventions

Sufentanil group:Intravenous injection of sufentanil
Osalidine group:Intravenous injection of oxaliplatin

Sponsors

Enze Hospital, Taizhou Enze Medical Center (Group)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age range of 18 to 80 years old; 2.ASA Level I-II; 3.BMI<30kg/m^2;

Exclusion criteria

Exclusion criteria: 1.Surgical time>30 minutes; 2.History of allergies to propofol, soybeans, or eggs; 3.Individuals with neurological and psychiatric disorders and those taking related medications; 4.Individuals with damage to target organs such as liver, kidney, heart, and brain; 5.Patients with language communication barriers who are unable to cooperate; 6.Past memory or cognitive impairment, sleep apnea syndrome, and difficult airway.

Design outcomes

Primary

MeasureTime frame
Patient and doctor satisfaction ratings;Record MAP, HR, and SpO2 at six different time points;

Secondary

MeasureTime frame
Comparison of Propofol Injection Pain;Total dosage of propofol;Anesthesia recovery status from the end of surgery to the patient's departure;Occurrence of nausea and vomiting within 24 hours after the examination;Occurrence of adverse events: intraoperative body movement, sinus bradycardia, hypotension;The patient's general condition, including sex, weight, age, height, and duration of examination;

Countries

China

Contacts

Public ContactXiang Haifei

Enze Hospital, Taizhou Enze Medical Center (Group)

xianghf@enzemed.com+86 576 89218166

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026