- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01045473
Prospective Study of Minimally Invasive Spine Surgery
January 8, 2010 updated by: Society for Minimally Invasive Spine Surgery
Prospective Study of Minimally Invasive Spinal Fusion Surgery for the Treatment of Spondylolisthesis, Degenerative Disk Disease, Spinal Stenosis and Degenerative Scoliosis
The population of the US is aging.
They remain more active and place greater demands on their musculoskeletal system.
A key problem is that pain and disability of age related spinal disorders will increase.
Problems such as Degenerative Lumbar Spondylolisthesis, Degenerative Disk Disease, Spinal Stenosis and Degenerative Scoliosis are age related problems that are treated with spinal fusion when non-operative treatment fails.
Traditional open surgery poses significant risk for patients in this age group.
The use of minimally invasive spinal surgery techniques provides an opportunity to treat these patients with less morbidity than traditional open surgery.
Study Overview
Status
Unknown
Study Type
Observational
Enrollment (Anticipated)
450
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Orthropedic surgeon's clinic.
Neurosurgeon's clinic.
Description
Inclusion Criteria: Inclusion Criteria:
- Patient age 21 - 90 years.
- Diagnosis of Spondylolisthesis, degenerative disk disease, and degenerative scoliosis (any curve magnitude).
- A spinal fusion is being undertaken via the minimally invasive approach.
- The patient agrees to follow-up for routine care for at least 2 years post-operatively.
Exclusion Criteria:
- Inability for post-operative follow-up
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2010
Primary Completion (Anticipated)
January 1, 2012
Study Completion (Anticipated)
June 1, 2012
Study Registration Dates
First Submitted
January 7, 2010
First Submitted That Met QC Criteria
January 8, 2010
First Posted (Estimate)
January 11, 2010
Study Record Updates
Last Update Posted (Estimate)
January 11, 2010
Last Update Submitted That Met QC Criteria
January 8, 2010
Last Verified
January 1, 2010
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- SMISS-001
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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