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Clinical Trial Summary

One hundred infantry recruits will be randomly assigned to two groups. Injuries will be monitored.


Clinical Trial Description

One hundred infantry recruits will be randomly assigned to receive experimental infantry boots (DEFINITE-REGULATOR) or standard issued boots (modified Belleville 390 TROP).

Overuse injuries and foot injuries will be monitored over a period of 14 weeks. The intervention group will wear experimental infantry boots and the controls will wear standard issue boots. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT02810002
Study type Interventional
Source Medical Corps, Israel Defense Force
Contact
Status Completed
Phase Phase 1/Phase 2
Start date August 2014
Completion date February 2015

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