Predicting the Outcome of Total Knee Arthroplasty and Spinal Surgeon

• Conditions: Osteoarthritis; Intervertebral Disc Degeneration

• Registration Number: NCT01989481
• Lead Sponsor: Beijing Jishuitan Hospital

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2013-11
• Study First Submitted: 2013-11-11
• Study First Submitted QC: 2013-11-15
• Study First Posted: 2013-11-21
• Status Verified: 2015-03
• Last Update Submitted: 2015-03-23
• Last Update Posted: 2015-03-24
• Primary Completion: 2015-12

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 2000

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.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

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

Secondary Outcome Measures

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

Trial Locations

Locations (1)

Beijing Hospital; 🇨🇳 Beijing, Beijing, China