Clinical Trials Directory

Trials / Terminated

TerminatedNCT01588730

Dynamic and Static Splinting as a Treatment for Plantar Faciiopathy

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
26 (actual)
Sponsor
Dynasplint Systems, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the Ankle Dorsiflexion Dynasplint System (DS) to static night splint for the reduction of pain from Plantar Fasciitis (Fasciopathy).

Conditions

Interventions

TypeNameDescription
DEVICEAnkle Dorsiflexion DynasplintDynamic Splinting utilizes the protocols of Low-Load, Prolonged-Duration Stretch (LLPS) with calibrated, adjustable tension to increase the Total End Range Time (TERT) to reduce contracture. This unit is worn at night while sleeping (6-8 hours) and, this does not affect activities of daily living
PROCEDURECommercially Available Static Night splintA commericially avilable static night splint will be worn for 4-6 hours during rest.

Timeline

Start date
2011-06-01
Primary completion
2015-06-01
First posted
2012-05-01
Last updated
2013-08-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01588730. Inclusion in this directory is not an endorsement.