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Research on the Application of Tegileridine for Postoperative Analgesia in Elderly Patients after Total Knee Arthroplasty

Research on the Application of Tegileridine for Postoperative Analgesia in Elderly Patients after Total Knee Arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115154
Enrollment
Unknown
Registered
2025-12-23
Start date
2025-12-25
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

Total knee arthroplasty

Interventions

Control Group (S Group, sufentanil 0.06 µg/kg·h + ondansetron 12mg + flurbiprofen ester 150mg + 0.9%NS,150ml in total):The group receive PCIA for postoperative analgesia after surgery, and set the dos
Low concentration group (T1 Group, tegileridine 0.9 µg/kg·h + ondansetron 12mg + flurbiprofen ester 150mg + 0.9%NS,150ml in total):The group receive PCIA for postoperative analgesia after surgery, and
Medium concentration group (T2 Group, tegileridine 1.2 µg/kg·h + ondansetron 12mg + flurbiprofen ester 150mg + 0.9%NS,150ml in total):The group receive PCIA for postoperative analgesia after surgery,
High concentration group (T3 Group, tegileridine 1.5 µg/kg·h + ondansetron 12mg + flurbiprofen ester 150mg + 0.9%NS,150ml in total):The group receive PCIA for postoperative analgesia after surgery, an

Sponsors

Lu'an Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Elderly patients undergoing elective total knee arthroplasty; 2. ASA classification I–III, age >= 65 years, and 18.5 <= BMI < 30; 3. Willing to participate in the study and have signed the informed consent form; 4. Capable of understanding and cooperating with the administration of questionnaires and scales used in this study.

Exclusion criteria

Exclusion criteria: 1. Those who are allergic to the study drug used in this experiment; 2. Those who have been taking sedative drugs and antipsychotic drugs for a long time; 3. Those who have been taking opioid drugs for a long time; 4. Patients with severe systemic diseases of the heart, brain, liver, kidneys, etc

Design outcomes

Primary

MeasureTime frame
Analgesic effect VAS score;Sedative effect Ramsay score;

Secondary

MeasureTime frame
PCIA press frequency within 48 hours after the operation ;

Countries

China

Contacts

Public ContactLi Renhu

Lu'an Hospital of Anhui Medical University

lirenhu2008@163.com+86 139 6624 1616

Outcome results

None listed

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