Screening and Prospective Cohort Study of Risk Factors for Enhanced Recovery After Spinal Fusion Surgery in Advanced Age Patient

Enrolling by invitationOBSERVATIONAL
Enrollment

500

Participants

Timeline

Start Date

September 3, 2024

Primary Completion Date

September 3, 2027

Study Completion Date

September 3, 2027

Conditions
Lumbar Disk HerniationLumbar Spinal StenosisLumbar SpondylolisthesisCervical Spondylotic MyelopathyCervical Radiculopathy
Interventions
DIAGNOSTIC_TEST

This is an observational study

This study divides the elderly population into two groups: the Elderly group and the Advanced age group. By observing the enhanced recovery after spinal fusion surgery in these two distinct age groups of elderly patients, risk factors affecting postoperative enhanced recovery will be identified. Detection index: Blood routine examination, blood biochemistry, coagulation function, imaging examination (X-ray, CT 3D reconstruction), Japanese Orthopaedic Association (JOA) score, visual analogue scale (VAS) pain score. The number of participants for all adverse events, serious adverse events, implant-related adverse events and drug-related serious adverse events, and the adverse events were summarized accordingly. The severity of adverse events will be rated according to NCI-CTCAE version 4.0.

Trial Locations (1)

430023

Department of Orthopedics, Affiliated Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430023, Wuhan

All Listed Sponsors
lead

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

OTHER