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Exploring the Safety and Efficacy of Tegileridine for Postoperative Analgesia in Elderly Patients Undergoing Hip Arthroplasty

Exploring the Safety and Efficacy of Tegileridine for Postoperative Analgesia in Elderly Patients Undergoing Hip Arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114979
Enrollment
Unknown
Registered
2025-12-19
Start date
2026-01-01
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

Elderly patients with hip fractures

Interventions

Control Group :Sufentanil was used for analgesia after the operation
Tegileridine Group:Postoperative analgesia was administered with Tegileridine

Sponsors

The First Affiliated Hospital of University of Science and Technology of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 86 Years

Inclusion criteria

Inclusion criteria: 1. Patients with hip fractures scheduled for elective total hip arthroplasty; 2. Aged >=65 years and 23 and Montreal Cognitive Assessment (MoCA) score >=26; 7. Voluntarily signed informed consent and willing to comply with the study protocol requirements.

Exclusion criteria

Exclusion criteria: 1. Patients with major organ or systemic diseases, uncontrolled hypertension, diabetes, coronary heart disease, or malignant tumors; 2. Patients with hypoalgesia or hyperalgesia, a history of chronic analgesic use, or a history of alcoholism; 3. Patients unable to complete postoperative MoCA and MMSE assessments, or with a history of psychiatric disorders; 4. Patients who have experienced any cerebrovascular events within the past 3 months, such as stroke or transient ischemic attack (TIA); 5. Patients with severe infections; 6. Patients with preoperative PaO2< 60 mmHg or SpO2< 92%; 7. Patients who have participated in another drug clinical trial within the past 30 days; 8. Patients who refuse to use a PCA pump for postoperative pain management; 9. Patients with a known allergy to the investigational drug(s).

Design outcomes

Primary

MeasureTime frame
The incidence of postoperative delirium;

Secondary

MeasureTime frame
Sleep quality assessment;Perioperative pain score;Postoperative adverse reactions;

Countries

China

Contacts

Public ContactMeng Yan

The First Affiliated Hospital of University of Science and Technology of China

ragingfire1988@163.com+86 190 5649 3287

Outcome results

None listed

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