Skip to content

Interactive Effect of Preoperative Frailty and Anesthesia Type on Postoperative Complications in Elderly Orthopedic Patients

Interactive Effect of Preoperative Frailty and Anesthesia Type on Postoperative Complications in Elderly Orthopedic Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121127
Enrollment
Unknown
Registered
2026-03-25
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Frailty and postoperative complications in elderly orthopedic patients

Interventions

General Anesthesia Group:General Anesthesia
Regional/Spinal-Epidural Anesthesia Group:Spinal or Epidural Anesthesia

Sponsors

Taihe County Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age >= 65 years; 2. Planned for elective or sub-emergency (e.g., hip fracture hospitalized within 48 hours) major lower limb orthopedic surgery (including: hip/knee arthroplasty, femur/tibia internal fixation); 3. Patient or family member provides informed consent and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Preoperative severe cognitive impairment (e.g., MMSE score = V or critically ill patients with expected survival <24 hours; 4. Severe hepatic or renal dysfunction (Child-Pugh C class or eGFR <15 mL/min/1.73m^2); 5. Participation in other clinical trials that may interfere with the results of this study.

Design outcomes

Primary

MeasureTime frame
30-day postoperative composite complication rate;

Secondary

MeasureTime frame
Postoperative length of stay;30-day all-cause readmission rate;30-day all-cause mortality rate;Time to first ambulation after surgery;Resting pain score;

Countries

China

Contacts

Public ContactZhang Fangfang

Taihe County Hospital of Traditional Chinese Medicine

365955644@qq.com+86 158 5585 6578

Outcome results

None listed

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