Retrospective Study of the Biomechanical Properties of Large Allografts
NCT ID: NCT00632294
Last Updated: 2012-08-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
2 participants
OBSERVATIONAL
2007-12-31
2009-09-30
Brief Summary
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1. To evaluate the material properties, histomorphometric indices, bone mineral density (BMD), and presence of microfractures in retrieved large allograft cortical bone specimens removed from orthopaedic oncology patients.
2. To correlate physical properties to patient demographics and medical treatment received.
Detailed Description
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As a standard of care, you will be having surgery to remove allograft tissue that has failed or because there were other complications following your earlier transplant. You will be separately consented for this surgery, which will describe the procedure and its risks in detail.
Tissue Research:
If you agree to take part in this study, leftover sample of the removed allograft bone will be collected and used to learn about the properties (such as bone strength, bone density, and new bone formation) of the removed transplant tissue. This tissue will be stored at the University of Arkansas for use in this study. Any remaining leftover tissue will be destroyed by the end of December 2011.
Data Collection:
Before you have surgery, you will have an x-ray. This is also part of standard of care. If you take part in this study, this x-ray will be used to learn about the properties of the transplant tissue.
All other information will be coming from your medical record, either from your past visits or as a result of your surgery. The information being collected will include information about your graft during the time it was within your body and observations made by your surgeon at its removal.
Length of Study:
Your participation in this study will be over after your tissue and data are collected.
This is an investigational study. Up to 200 patients will be enrolled on this multicenter study. Up to 20 will be enrolled at M. D. Anderson.
Conditions
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Keywords
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Study Design
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CASE_ONLY
RETROSPECTIVE
Study Groups
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Retrieved Allograft
Patients that require the retrieval of a bone allograft (transplant).
Tissue Sample
A leftover sample of the removed allograft bone will be collected.
Interventions
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Tissue Sample
A leftover sample of the removed allograft bone will be collected.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
ALL
No
Sponsors
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Musculoskeletal Transplant Foundation
OTHER
M.D. Anderson Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Valerae O. Lewis, MD
Role: PRINCIPAL_INVESTIGATOR
M.D. Anderson Cancer Center
Locations
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U.T.M.D. Anderson Cancer Center
Houston, Texas, United States
Countries
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Related Links
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MD Anderson Cancer Center
Other Identifiers
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2007-0689
Identifier Type: -
Identifier Source: org_study_id