Predicting the Outcome of Total Knee Arthroplasty and Spinal Surgeon

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

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01989481

Enrollment

2000

Registered

2013-11-21

Start date

2013-11-30

Completion date

Unknown

Last updated

2015-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intervertebral Disc Degeneration, Osteoarthritis;

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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy volunteers

Inclusion criteria

1. The patients have been waiting for surgery for treatment of osteoarthritis or disc degeneration disease. 2. Must be between 18 and 65 years of age, of either sex. 3. Must demonstrate willingness to participate in the study by signing the written informed consent.

Exclusion criteria

1. Patients with Mandatory spondylitis, infections, neoplasms, inflammation, deformities, or previous surgery of spine or knee. 2. The patient is participating in an interventional clinical trial or has in an interventional clinical trial within 30 days prior to enrollment.

Design outcomes

Primary

Measure	Time frame
Change of functional score over time in the patients after operation	3, 6, 12 months after surgery

Secondary

Measure	Time frame
Change of quality of life score over time in the patients after operation	3, 6, 12 monthes after surgery

Countries

China

Contacts

Primary ContactChengai Wu, Doctor

wuchengai05@163.com+86-010-58516611

Outcome results