Status:
ENROLLING_BY_INVITATION
Screening and Prospective Cohort Study of Risk Factors for Enhanced Recovery After Spinal Fusion Surgery in Advanced Age Patient
Lead Sponsor:
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Conditions:
Lumbar Disk Herniation
Lumbar Spinal Stenosis
Eligibility:
All Genders
60+ years
Brief Summary
To determine the high risk factors affecting accelerated recovery after spinal fusion surgery in advanced age patient.
Detailed Description
To determine the high risk factors affecting accelerated recovery after spinal fusion surgery in elderly patients: a prospective cohort study
Eligibility Criteria
Inclusion
- Informed consent signed and dated by subject or guardian
- Commit to follow the research procedures and cooperate with the whole process of the study
- The subjects are 60 years old or older, regardless of gender
- Patients with degenerative spinal diseases requiring spinal fusion surgery
- Generally in good physical condition
- Able to adhere to and cooperate with research interventions, such as oral medication
- In fertile women, contraception should be used for at least one month prior to screening, and they should commit to use contraception throughout the study period and continue until the specified time after the study
Exclusion
- Acute infection
- Congenital malformation
- Abnormal anatomy or skeletal variation
- Malignant tumor
- The surgical area was locally infected with symptoms of local inflammation
- Fever or leukocytosis
- Morbid obesity
- Pregnant and nursing women
- Mental illness
- Acute joint disease, bone resorption, osteopenia and/or osteoporosis. Osteoporosis is a relative contraindication, as this condition may limit the degree of correction that can be produced, the amount of mechanical fixation, and/or the quality of the bone graft
- Patients who are unwilling to cooperate with post-operative treatment
- Any time an implant is performed it interferes with the anatomy or intended physiological function of the patient
Key Trial Info
Start Date :
September 3 2024
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
September 3 2027
Estimated Enrollment :
500 Patients enrolled
Trial Details
Trial ID
NCT06591442
Start Date
September 3 2024
End Date
September 3 2027
Last Update
September 19 2024
Active Locations (1)
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1
Department of Orthopedics, Affiliated Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430023
Wuhan, Hubei, China, 430023