NCT01989481UnknownNot Applicable
Prospective Study of Risk Factors and Outcomes Following Total Knee Arthroplasty and Spinal Surgeon
Beijing Jishuitan Hospital1 site in 1 country2,000 target enrollmentStarted: November 2013Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Sponsor
- Beijing Jishuitan Hospital
- Enrollment
- 2,000
- Locations
- 1
- Primary Endpoint
- Change of functional score over time in the patients after operation
Study Overview
Brief Summary
The purpose of this observational study is to investigate the preoperative and operative factor of pain and functional outcome at one years following total knee arthroplasty and spinal surgeon.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to 65 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •The patients have been waiting for surgery for treatment of osteoarthritis or disc degeneration disease.
- •Must be between 18 and 65 years of age, of either sex.
- •Must demonstrate willingness to participate in the study by signing the written informed consent.
Exclusion Criteria
- •Patients with Mandatory spondylitis, infections, neoplasms, inflammation, deformities, or previous surgery of spine or knee.
- •The patient is participating in an interventional clinical trial or has in an interventional clinical trial within 30 days prior to enrollment.
Outcomes
Primary Outcomes
Change of functional score over time in the patients after operation
Time Frame: 3, 6, 12 months after surgery
Secondary Outcomes
- Change of quality of life score over time in the patients after operation(3, 6, 12 monthes after surgery)
Investigators
Wei Tian
Director of Beijing Jishuitan Hospital
Beijing Jishuitan Hospital
Study Sites (1)
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