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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00843973
Other study ID # IRB 1095798
Secondary ID
Status Completed
Phase N/A
First received January 26, 2009
Last updated June 20, 2017
Start date June 2008
Est. completion date December 2013

Study information

Verified date June 2017
Source University of Missouri-Columbia
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to find out if the cells in bone graft samples collected using a reamer are similar to the cells in bone graft samples collected using the iliac crest bone graft method.


Description:

Although iliac crest bone grafting is the gold standard for autogenous bone grafting procedures, limited quantity in some individuals and donor site morbidity have lead surgeons to look for alternative harvest sites or sources such as allograft or osteobiologics. Of these alternative harvest sites is the femoral shaft. Intramedullary contents from reaming are composed of bone marrow, and blood and bone spicules. In this respect, the reamed contents are similar to the bone routinely harvested from the iliac crest. Studies have shown that despite the reaming process using standard reamers, cells maintain their viability and are able to produce new bone. However, the addition of aspiration and irrigation used in the RIA system could potentially compromise the harvested cell viability and limit their osteogenic potential. In addition, Wenisch et al. have concluded that the harvested cells using standard intramedullary reamers not only proceed toward osteogenic differentiation, but also can be directed toward neurogenic differentiation. This suggests that reaming debris is a viable source of stem cells as well. RIA allows for these cells to be harvested. It is our hypothesis that the intramedullary contents harvested using the RIA system is similar to ICBG in cell viability and osteogenic potential.


Recruitment information / eligibility

Status Completed
Enrollment 83
Est. completion date December 2013
Est. primary completion date October 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Subjects age 18 years or older

- Subjects undergoing a bone grafting procedure, either using an iliac crest or RIA system harvesting technique, or

- Subjects undergoing reamed femoral intramedullary nailing using the RIA reaming technique

Exclusion Criteria:

- Subjects under age 18

- Subjects with a history of: leukemia; cancer with bone metastases; renal failure, receiving dialysis; or on immunosuppressive medications

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
iliac crest bone graft
iliac crest bone graft procedure
Reamer Irrigator Aspirator
Reamer Irrigator Aspirator (RIA) Procedure

Locations

Country Name City State
United States University of Missouri Columbia Missouri

Sponsors (2)

Lead Sponsor Collaborator
University of Missouri-Columbia AO North America

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cell viability 1 hour post-collection
Primary Osteogenic potential 1 hour post-collection
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