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Oliceridine Combined with Esketamine Improves Analgesic Efficacy and Safety in Elderly Patients After Laparoscopic Colorectal Cancer Surgery: A Randomized Controlled Study

Oliceridine Combined with Esketamine Improves Analgesic Efficacy and Safety in Elderly Patients After Laparoscopic Colorectal Cancer Surgery: A Randomized Controlled Study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115708
Enrollment
Unknown
Registered
2025-12-30
Start date
2025-03-05
Completion date
Unknown
Last updated
2026-01-05

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 (Group O):Patient-controlled intravenous analgesia (PCIA) with oliceridine alone. The PCIA solution contains oliceridine 20 mg diluted in normal saline to 100 mL. The pump is set wit
Esketamine Group (Group E):Patient-controlled intravenous analgesia (PCIA) with esketamine alone. The PCIA solution contains esketamine 100 mg diluted in normal saline to 100 mL. The pump is set with
Oliceridine + Esketamine Combination Group (Group OE):Patient-controlled intravenous analgesia (PCIA) with a combination of oliceridine and esketamine. The PCIA solution contains oliceridine 20 mg and

Sponsors

Henan University Huaihe Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 65–80 years; 2. Scheduled for elective laparoscopic radical resection of colorectal cancer; 3. ASA physical status II–III; 4. Informed consent obtained.

Exclusion criteria

Exclusion criteria: 1. History of drug allergy; 2. Severe hepatic or renal insufficiency; 3. History of chronic pain or long-term opioid use; 4. Severe psychiatric or cognitive disorders; 5. History of drug or alcohol abuse; 6. Conversion to open surgery or occurrence of severe intraoperative complications.

Design outcomes

Primary

MeasureTime frame
Postoperative active pain score;

Secondary

MeasureTime frame
Total consumption of oliceridine within 48 hours post-operation;Postoperative adverse reaction incidence rate;Postoperative Recovery Quality Score;Number of compressions of analgesic pump;First anal exhaust time after surgery;Post hospitalization duration;

Countries

China

Contacts

Public ContactLimin Liang

Henan University Huaihe Hospital

qazwsx3337597@163.com+86 182 3658 0656

Outcome results

None listed

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