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The effect of oxelidine versus hydromoradone for multimodal analgesia on postoperative recovery in patients undergoing colorectal surgery: A single-center, randomized, double-blind, controlled study

The effect of oxelidine versus hydromoradone for multimodal analgesia on postoperative recovery in patients undergoing colorectal surgery: A single-center, randomized, double-blind, controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111369
Enrollment
Unknown
Registered
2025-10-30
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

Colorectal cancer

Interventions

Oliceridine group:0.4mg/kg of oliceridine plus saline to 100ml
Hydromorphone group:0.1 mg/kg of hydromorphone plus saline to 100ml

Sponsors

Peking University Shougang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18–70 years old; 2. ASA grade I–III; 3. Undergoing colorectal cancer surgery under general anesthesia (with a midline incision >5 cm); 4. BMI is 18.5–29.9 kg/m^2 [BMI = weight (kg) / height (m)^2]; 5. The patient selects an analgesic pump for postoperative analgesia; 6. Ethical compliance, voluntary patient participation, and informed consent signed by the patient prior to surgery.

Exclusion criteria

Exclusion criteria: 1. Individuals who are allergic to the study drug; 2. Individuals with severe abnormalities in liver and kidney function (severe liver dysfunction: ALT, conjugated bilirubin, AST, ALP, total bilirubin, any of which is greater than twice the upper limit of normal; severe renal dysfunction: creatinine clearance rate <30 ml/min); 3. Patients with New York Heart Association Class II or above; 4. Individuals with severe respiratory diseases; 5. Individuals with a history of chronic pain; 6. Individuals with infection at the injection site; 7. Individuals with alcohol or drug abuse; 8. Individuals with opioid dependence; 9. Individuals with mental illnesses that interfere with pain perception and assessment.

Design outcomes

Primary

MeasureTime frame
QoR-15 score 24 hours after surgery;

Secondary

MeasureTime frame
QoR-15 scores at 48 hours and 72 hours after surgery;Pain scores during postoperative rest and activity;Postoperative rescue analgesic dose;Adverse reactions associated with opioids (nausea, vomiting, respiratory depression, itching, dizziness);Time of first getting out of bed;Time of intestinal function recovery;

Countries

China

Contacts

Public ContactZhao Lin

Peking University Shougang Hospital

yam_0106@163.com+86 135 2253 1376

Outcome results

None listed

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