- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03859609
Comparison of GAP-score With Schwab-score
August 14, 2019 updated by: Mohammad ARAB MOTLAGH
Failure Prediction of Adult Spinal Deformity Surgery Comparing GAP-score With Schwab-score
The predictive value of two different score-systems with regard to failure rate following long extent spinal fusion is subject of evaluation.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The multilevel spinal fusion is associated with high rate of failure.
This results from insufficient adaptation of the fused spine to the proper individual spinal alignment.
In the recent years, comprehensive understanding of spinal alignment and definition of several parameters contributed to develop score systems to evaluate the alignment of the multilevel spinal fusion and to predict failure.
In the following study the results of multilevel spinal fusion were evaluated retrospectively according to two scoring systems: GAP-score und Schwab-score.
The predictive value of each score system is analyzed by the correlation of the failure rate with its corresponding score value.
Study Type
Observational
Enrollment (Actual)
94
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Frankfurt, Germany, 60528
- Department of Orthopaedic Surgery, University Hospital Frankfurt
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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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients who had fusion operation with dorsal instrumentation on at least 3 spinal levels
Description
Inclusion Criteria:
- 3 and more fusion levels
Exclusion Criteria:
- Neuromuscular disease
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
- Observational Models: Cohort
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Radiological Evaluation
Time Frame: 2 months
|
Pelvic tilt in degree, Pelvic incidence in degree, Sacral slope in degree, Lumbar lordosis in degree, L5-S1 lordosis in degree, Thoracic kyphosis in degree, Sagittal vertical axis in degree, Thoracolumbar kyphosis in degree, Global tilt in degree, Cobb angle in degree
|
2 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Mohammad Arab Motlagh, MD, PhD, University Hospital Frankfurt
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 (Actual)
March 1, 2019
Primary Completion (Actual)
April 30, 2019
Study Completion (Actual)
June 30, 2019
Study Registration Dates
First Submitted
February 27, 2019
First Submitted That Met QC Criteria
February 28, 2019
First Posted (Actual)
March 1, 2019
Study Record Updates
Last Update Posted (Actual)
August 16, 2019
Last Update Submitted That Met QC Criteria
August 14, 2019
Last Verified
August 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- Adult Spinal Deformity Surgery
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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