Clinical Study of the L300 Versus Ankle-foot Orthosis (AFO) on Post-Stroke Subjects With Foot Drop

NACompletedINTERVENTIONAL
Enrollment

197

Participants

Timeline

Start Date

May 31, 2010

Primary Completion Date

December 31, 2012

Study Completion Date

February 28, 2013

Conditions
Sensorimotor Gait DisorderNeurologic Ambulation DisorderGait, Drop FootPoststroke HemiparesisPost-Cerebrovascular Accident (CVA) Hemiparesis
Interventions
DEVICE

Ness L300

The Ness L300 delivers functional electrical stimulation (FES), which improves gait function, stroke-specific quality of life, functionality, and safety for persons with stroke.

DEVICE

Ankle-foot orthosis

"The Control Group will walk with a usual ankle-foot orthosis (AFO)."

Trial Locations (11)

10065

Weill Cornell Medical Center, New York

11777

St.Charles Hospital & Rehabilitation, Port Jefferson

20010

National Rehabilitation Hospital, Washington D.C.

32216

Brooks Center for Rehabilitation Studies, Jacksonville

45216

The Drake Center /University of Cincinnati, Cincinnati

66160

Kansas University Medical Center, Kansas City

84132

University of Utah, School of Medicine, Salt Lake City

90806

Long Beach Memorial Medical Center, Long Beach

92123

Sharp Rehabilitation Center, San Diego

90242-3496

Rancho Los Amigos National Rehabilitation Center, Downey

75390-9055

UT Southwestern, Dallas

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Medidata Solutions

INDUSTRY

collaborator

University of Cincinnati

OTHER

lead

Bioness Inc

INDUSTRY