CompletedNot Applicable

Pre-operative Risk Assessment Combined With Targeted Intervention in the Chinese Elderly With Spine Surgery

China164 participantsStarted 2024-04-15

Plain-language summary

With the extended life expectancy of the Chinese population and improvements in surgery and anesthesia techniques, the number of aged patients undergoing surgery has been increasing annually. However, safety, effectiveness, and quality of life of aged patients undergoing surgery are facing major challenges. This prospective, multi-center, randomized, controlled study aims to construct a prehabilitation combined with enhanced recovery after surgery program which includes pre-operative risk assessment and targeted intervention.

Who can participate

Age range75 Years

SexALL

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Inclusion criteria

✓. patients who voluntarily sign the informed consent form; (2) elective spinal fusion surgery for degenerative spinal disorders; (3) no severe cognitive impairment (MoCA score ≥ 8).

Exclusion criteria

✕. have urgent condition that needs to be managed before the surgery,
✕. are unable to cooperate with preoperative assessment,
✕. have spinal fractures, metastasis, and spinal infections,
✕. unable to understand or participate safely in intervention program,
✕. participate in another study that may affect the study.

What they're measuring

Comprehensive Complication Index

Timeframe: up to 90 days after surgery

Trial details

NCT IDNCT06140797

SponsorXuanwu Hospital, Beijing

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-09-10

View on ClinicalTrials.gov More Spine Degeneration trials