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Oliceridine Combined with Esketamine for Postoperative Analgesia in Elderly Patients Undergoing Laparoscopic Colorectal Cancer Surgery: A Prospective Randomized Controlled Trial

Oliceridine Combined with Esketamine for Postoperative Analgesia in Elderly Patients Undergoing Laparoscopic Colorectal Cancer Surgery: A Prospective Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122211
Enrollment
Unknown
Registered
2026-04-10
Start date
2026-04-15
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

colorectal cancer

Interventions

OS(Oliceridine + Sufentanil):Oliceridine 0.35 mg/kg + Sufentanil 1 µg/kg, patient-controlled intravenous analgesia (PCIA) for 48 hours postoperatively. Background infusion 2 mL/h, bolus 0.5 mL, lockou
OE(Oliceridine + Esketamine):Oliceridine 0.35 mg/kg + Esketamine 1 mg/kg in 100 mL saline. PCIA: background 2 mL/h, bolus 0.5 mL, lockout 15 min. Each bolus: oliceridine 1.75 µg/kg + esketamine 5 µg/k

Sponsors

Henan University Huaihe Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age: 65 to 80 years. 2. Scheduled surgery: Elective laparoscopic radical resection of colorectal cancer. 3. Body mass index (BMI): 18.5 to 30.0 kg/m2. 4. Voluntary participation: Ability to provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. History of drug allergies; 2. Severe liver or kidney dysfunction; 3. History of chronic pain or long-term use of opioid drugs; 4. Severe mental or cognitive disorders; 5. History of substance or alcohol abuse; 6. Conversion to open surgery during operation or occurrence of serious 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 ContactLiang Limin

Henan University Huaihe Hospital

kflxwang@163.com+86 182 3658 0656

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026