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Clinical Trial Summary

This is a prospective, randomized, control, open label study in which up to 50 subjects with metatarsus adductus (MTA) will be enrolled. Subjects will be treated with the standard casting or using the UNFO-s device for total time of 20 weeks.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01600183
Study type Interventional
Source Unfo Ltd.
Contact Dan Atar, Prof
Phone 972-506264277
Email dan_atar@yahoo.com
Status Not yet recruiting
Phase N/A
Start date August 2012

See also
  Status Clinical Trial Phase
Recruiting NCT05587569 - Outcomes Following Combined Adductoplasty™ and Lapiplasty® (MTA3D) N/A