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NCT Number: NCT00623389

Evaluation of an Advanced Lower Extremity Neuroprostheses

The purpose of this study is to evaluate a surgically implanted functional electrical stimulation (FES) system to facilitate exercise, standing, stepping and/or balance in people with various degrees of paralysis.

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Key information

Age range

21 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Louis Stokes Cleveland VA Medical Center, Cleveland, Ohio, United States

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About this study

Protocol Outline: Patents undergo surgery in which electrodes are implanted into muscles of the trunk and legs. Electrode leads are connected to an stimulator/telemeter. Following implantation, patients undergo training in standing, transfers and other advanced mobility skills using the functional electrical stimulation system. A prescribed course of exercise, functional training and rehabilitation with the implanted stimulation system, followed by laboratory assessments of strength, balance and functional abilities with and without the system, as well as the technical performance of the implanted components. Home-based training follows prior to discharge for home use of the system.

Patients are followed at 6 and 12 months after discharge and then annually thereafter.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Phase I Inclusion Criteria

  • Skeletal maturity and ability to sign informed consent (>18 years)
  • Non-ventilator dependent paralysis resulting from injuries such as: mid cervical/thoracic (C4 or below) spinal cord injuries, poststroke hemiparesis, TBI, or MS, affecting the trunk and/or lower limbs
  • Innervated and excitable lower extremity and trunk musculature
  • Adequate social support and stability
  • Willingness to comply with follow-up procedures

Phase I Exclusion Criteria

  • Non-English speaking
  • Females who are pregnant
  • Current pressure injuries that would be exacerbated by study activities
  • Severe contractures or uncontrolled spasticity of any major joint of the upper or lower extremities that results in a fixed deformity that would interfere with study activities
  • History of spontaneous fractures or other evidence of excessively low bone density
  • History of vestibular dysfunction, balance problems, or spontaneous falls
  • Acute and or/untreated orthopedic problems that would prevent a participant from weight bearing or exercising such as a dislocation or fracture.

Treatment and study plan

IST (Implanted Stimulator-Telemeter)

Device

Pre-surgical exercise with surface electrical stimulation, surgery including electrode and IST- implanted pulse generator insertion, exercise and physical therapy with the implanted system, functional training and laboratory assessment of clinical and technical performance.

Primary outcomes

  1. Device reliability and technical performance measuring changes in standing duration from baseline at discharge to 12 months after discharge

    Time frame: Change from immediately after intervention and 1 year after intervention

    Repeated measures of standing duration in minutes

  2. Device reliability and technical performance measuring changes in standing loads from baseline at discharge to 12 months after discharge

    Time frame: Change from immediately after intervention and 1 year after intervention

    Repeated measures of arm/leg loading measured in Kg

  3. Device reliability and technical performance measuring changes in walking distance from baseline at discharge to 12 months after discharge

    Time frame: Change from immediately after intervention and 1 year after intervention

    Repeated measures of walking distance in meters

  4. Device reliability and technical performance measuring changes in walking duration from baseline at discharge to 12 months after discharge

    Time frame: Change from immediately after intervention and 1 year after intervention

    Repeated measures of walking time in minutes

Secondary outcomes

  1. Device operability measuring changes in functional activities of daily living from baseline at discharge and 12 months after discharge

    Time frame: Change from immediately after intervention and 1 year after intervention

    Repeated measures of standing reach in cm, and transfer height in cm

Study contacts

Contact information is provided by the study sponsor or research team.

Lisa M Lombardo, MPT

CONTACT

[email protected]

216-791-3800 ext. 64909

Maura Malenchek, PTA

CONTACT

[email protected]

216-791-3800 ext. 64989

Sponsors and collaborators

Lead sponsor

Case Western Reserve University

Other

Registry information

Official study title

Evaluation of Advanced Lower Extremity Neuroprostheses

Acronym: LE-IST

Important dates

Study start
2018
Primary completion
2027
Study completion
2027
First posted
Feb 26, 2008
Registry last updated
Jul 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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