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Oliceridine for postoperative analgesia in adults with lower limb fractures: a randomized, controlled, double-blind clinical study

Oliceridine for postoperative analgesia in adults with lower limb fractures: a randomized, controlled, double-blind clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094117
Enrollment
Unknown
Registered
2024-12-17
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Acute postoperative pain

Interventions

Group Oliceridine:Oliceridine
Group Fentanil:Fentanil

Sponsors

Chongqing Emergency Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Undergoiong unilateral lower extremity fracture operation; 2.Age between 18 years old and 65 years old; 3.ASA Grade I - III; 4.BMI=18-35kg/m2; 5.Operation time between 1 hour and 3 hours;

Exclusion criteria

Exclusion criteria: 1.Opioid allergy and recent use of opioids; 2.Patients with opioid contraindications; 3.Pregnant and lactating women; 4.Abnormal mental or neurological function; 5.Patients with major organ dysfunction: NYHA cardiac function grade =?; Pulmonary function grade of COPD patients =?; The Child-Pugh grade of liver function reached B and C grades. eGFR<60ml/min; 6.Patients with pain in other areas; 7.Patients reject to participate in this study;

Design outcomes

Primary

MeasureTime frame
48-hour postoperative NRS;

Countries

China

Contacts

Public ContactHong Fu

Chongqing Emergency Medical Center

13018396185@163.com+86 23 63692144

Outcome results

None listed

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