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NCT01817179 · ClinicalTrials.gov registry record · NA

Functional Electrical Stimulation for Hemiplegic Cerebral Palsy

A NA study, sponsored by Children's Hospital Medical Center, Cincinnati.

Completed
Registry status
NA
Development phase
12
Enrollment target

NCT01817179: Completed NA study, sponsored by Children's Hospital Medical Center, Cincinnati.

NCT01817179 is a NA study that has completed, run by Children's Hospital Medical Center, Cincinnati. The registered enrollment target is 12 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01817179, a NA study, has completed, sponsored by Children's Hospital Medical Center, Cincinnati.

COMPLETED
Registry status
NA
Development phase
12 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate how a functional electrical stimulation (FES) device worn on the lower leg effects how children (ages 6-17 years) with hemiplegic cerebral palsy walk and perform other functional activities. The investigators expect to find that wearing the functional electrical stimulation device will improve walking and other functional activities of children with hemiplegic cerebral palsy. Participants will be trained in use of the device and will be required to wear it daily for 3 months. Each participant will be evaluated before beginning the intervention and after completing the intervention. This study will provide important information regarding the benefits of this treatment intervention in children with hemiplegic cerebral palsy.

Interventions

  • OTHER FES neuroprosthesis to dorsiflexors on affected leg

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2013-03
Est. Completion 2014-12
Phase NA

What the finished NCT01817179 record still lists

NCT01817179 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which FES neuroprosthesis to dorsiflexors on affected leg is the first listed.

NCT01817179 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01817179 about?

NCT01817179 is a clinical study titled "Functional Electrical Stimulation for Hemiplegic Cerebral Palsy". The purpose of this study is to evaluate how a functional electrical stimulation (FES) device worn on the lower leg effects how children (ages 6-17 years) with hemiplegic cerebral palsy walk and perform other functional activities. The investigators expect to find that wearing the functional electr...

What is the current status of trial NCT01817179?

This trial is currently completed. It is a NA study. The enrollment target is 12 participants. The study started on 2013-03. Estimated completion is 2014-12.

What interventions are being tested in trial NCT01817179?

The interventions under investigation include: FES neuroprosthesis to dorsiflexors on affected leg (OTHER).

Who is sponsoring clinical trial NCT01817179?

This trial is sponsored by Children's Hospital Medical Center, Cincinnati, which has 571 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01817179's enrollment target sits among peer trials

12 1913th of 2000 higher than 74 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01817179, the US trial registry maintained by the National Library of Medicine. NCT01817179 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.