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Clinical Trials/NCT01989481
NCT01989481
Unknown
N/A

Prospective Study of Risk Factors and Outcomes Following Total Knee Arthroplasty and Spinal Surgeon

Beijing Jishuitan Hospital1 site in 1 country2,000 target enrollmentNovember 2013

Overview

Phase
N/A
Intervention
Not specified
Conditions
Osteoarthritis;
Sponsor
Beijing Jishuitan Hospital
Enrollment
2000
Locations
1
Primary Endpoint
Change of functional score over time in the patients after operation
Last Updated
11 years ago

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.

Registry
clinicaltrials.gov
Start Date
November 2013
End Date
December 2015
Last Updated
11 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Wei Tian

Director of Beijing Jishuitan Hospital

Beijing Jishuitan Hospital

Eligibility Criteria

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)

Study Sites (1)

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