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Clinical Study of Oliceridine in Outpatient Elderly Patients Undergoing Cystoscopy

Clinical Study of Oliceridine in Outpatient Elderly Patients Undergoing Cystoscopy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100520
Enrollment
Unknown
Registered
2025-04-10
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-04-14

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

Conditions

Cystoscopic examination

Interventions

Group O1:Oliceridine0.5mg intravenously
Group O2:Oliceridine1mg intravenously
Group S:Sufentanil 50ug intravenously

Sponsors

The Second Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients whose initial clinical diagnosis is consistent with cystoscopy or treatment indications; Age 60-75 years old; American Society of Anesthesiologists (ASA) grade?—?, and Mallampati airway grade I~?.

Exclusion criteria

Exclusion criteria: There is a serious systemic disease; Allergies to drugs used in this study have a history of alcohol or sedative and analgesic drug abuse; Unable to give fully informed consent due to intellectual or behavioral disabilities; No recent history of cold; No recent anticoagulant medication.

Design outcomes

Primary

MeasureTime frame
NRS Score;Incidence of moderate to severe urinary tract irritation;

Secondary

MeasureTime frame
Sedation success rate;Success rate of lens insertion;Propofol dosage (mg) ;Inspection time (min) ;Incidence of hypoxemia;Incidence of urinary tract irritation ;Incidence of postoperative nausea and vomiting;propofol supplemental times;wake up time (min);

Countries

China

Contacts

Public ContactZhao Peng

The Second Hospital of Jilin University

zhaopeng8933@126.com+86 135 0430 8933

Outcome results

None listed

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