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A Study on the Application of Tegileridine in Postoperative Pain Management for Elderly Patients with Hip Fractures

A Study on the Application of Tegileridine in Postoperative Pain Management for Elderly Patients with Hip Fractures

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600129211
Enrollment
Unknown
Registered
2026-08-01
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Hip fracture in the elderly

Interventions

Trial group:For the patients in the experimental group, 1 mg of tegretol was administered intravenously as the loading dose, which was infused within 10 minutes. It was combined with PCIA, with a conc
Control group:For the control group patients, sufentanil 0.1 µg/kg was added at the end of the surgery, combined with PCIA, with a sufentanil concentration of 2 µg/ml, totaling 100 ml. The background

Sponsors

Department of Anesthesiology, Sinopharm Gezhouba Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.ASA grade II-III; 2. for patients over 65 years old who plan to undergo hip fracture surgery under general anesthesia, either artificial femoral head replacement or anti-rotation intramedullary nails can be used as surgical methods.

Exclusion criteria

Exclusion criteria: 1.ASA grade III or above; 2.emergency patients; 3.New York Heart Function Classification (NYHA) grade 3-4; 4.cardiac conduction block (sinus node conduction block or atrioventricular conduction block); 5.gastric ulcer; 6.body mass index (BMI) > 37 kg/m2; 7. patients with poorly controlled diabetes treated with insulin; 8.kidney diseases; 9.liver diseases; 10.patients with blood clotting disorders or those taking warfarin, new anticoagulants such as rivaroxaban or dabigatran due to other disease reasons; 11.patients who have engaged in heavy drinking or have severe dependence on narcotic and psychotropic drugs in the past two months; 12.patients with uncontrollable anxiety, schizophrenia or other mental disorders.

Design outcomes

Primary

MeasureTime frame
Area under the pain score curve at 48 hours postoperatively;

Secondary

MeasureTime frame
The number of PCA iterations;Recovery of analgesic effect frequency within 0–48 hours;IL-6;IL-8;First PCA time;

Countries

China

Contacts

Public ContactZhan Weiwei

Sinopharm Gezhouba Central Hospital

504461407@qq.com+86 136 1717 8509

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026