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Clinical Trial Summary

A prospective, randomised study is to investigate the feasibility of conducting a superiority randomised controlled trial comparing the application of combined autologous PRP and concentrated autologous bone marrow (PRP-BMA) in addition to standard of care (either reamed intramedullary nailing or fine wire ring external fixator) for patients presenting with fresh tibial diaphyseal fractures.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03100695
Study type Interventional
Source University of Leeds
Contact
Status Active, not recruiting
Phase N/A
Start date October 4, 2018
Completion date December 31, 2021