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A retrospective comparative study of the postoperative analgesia effects of oxycodone and tagelil in patients undergoing abdominal surgery

A retrospective comparative study of the postoperative analgesia effects of oxycodone and tagelil in patients undergoing abdominal surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600125335
Enrollment
Unknown
Registered
2026-05-25
Start date
2026-05-25
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Pain

Interventions

Exposure group: Oxycodone group
Non-exposure group: Tajiridine group:NA

Sponsors

Fifth Affiliated Hospital, Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.Over 18 years old; 2.Gender not limited; 3.From April 2025 to April 2026, the patient received treatment at the Fifth Affiliated Hospital of Sun Yat-sen University; 4.Those who have undergone elective or emergency abdominal surgery; 5.Postoperative analgesia was administered using patient-controlled intravenous analgesia (PCIA), with oxycodone or tajiridin being the primary analgesic drugs; 6.Postoperative hospital stay >=48 hours;

Exclusion criteria

Exclusion criteria: 1.Patients with a history of chronic pain before surgery and long-term use of opioids (>=3 months or daily oral morphine equivalent dose >30mg); 2.Known allergy to oxycodone or tegafur; 3.Severe hepatic impairment (Child-Pugh C) or renal impairment (eGFR < 30 mL/min/1.73m²); 4.Patients with preoperative chronic respiratory failure (resting SpO2 < 90% or requiring home oxygen therapy) or uncontrolled obstructive sleep apnea (AHI = 30) were admitted to the hospital. 5.Uncontrolled mental illness (such as major depressive disorder, schizophrenia) or history of substance abuse; 6.Reoperation is required during or within 24 hours after surgery due to bleeding, anastomotic leakage, or other reasons. 7.Postoperatively transferred to the ICU and mechanically ventilated for more than 24 hours;

Design outcomes

Primary

MeasureTime frame
Pain scores at rest and during activity within 48 hours post-surgery;

Secondary

MeasureTime frame
Post-operative nausea and vomiting;

Countries

China

Contacts

Public ContactYing Wang

Fifth Affiliated Hospital, Sun Yat-Sen University

wangying851208@163.com+86 187 5012 9581

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026