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NCT00289393 Clinical Trial

Response Shift in Patient Expectations and Functional Outcome

Spinal Injuries Clinical Trial

Official title:
Response Shift in Patient Expectations and Functional Outcome Following Posterior Lumbar Spinal Surgery for Degenerative Spinal Disorders

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00289393
Other study ID # REB #151-2004
Secondary ID
Status Recruiting
Phase N/A
First received February 8, 2006
Last updated September 11, 2006

Study information
Verified date September 2006
Source Sunnybrook Health Sciences Centre
Contact Nana Adjei
Phone 416-480-6100
Email nana.adjei@sunnybrook.ca
Is FDA regulated No
Health authority Canada: Health Canada
Study type Observational

Clinical Trial Summary

The purpose of this study is to evaluate the results of elective lumbar spinal surgery as it relates to shifting patient expectations for outcome. Patients undergoing elective posterior spinal surgery for degenerative conditions of the spine at SWCHSC will be evaluated.

Recruitment information / eligibility
Status Recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- All patients with a diagnosis of a degenerative condition of the lumbar spine undergoing posterior lumbar spinal surgery at Sunnybrook and Women's College Health Sciences Centre

- Patients who have had previous lumbar surgery

Exclusion Criteria:

- Traumatic or neoplastic surgical conditions of the lumbar spine

Study Design

Observational Model: Defined Population, Time Perspective: Longitudinal

Related Conditions & MeSH terms

Intervention

Behavioral:
• Perceived outcome by both patient and physician

Locations
Country Name City State
Canada Sunnybrook Health Sciences Centre Toronto Ontario

Sponsors (1)
Lead Sponsor Collaborator
Sunnybrook Health Sciences Centre

Country where clinical trial is conducted

Canada, 

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