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NCT03249454 · ClinicalTrials.gov registry record · NA

Effects of Transcutaneous Spinal Direct Current Stimulation in Incomplete Spinal Cord Injury

A NA study, sponsored by The University of Texas Health Science Center, Houston.

Completed
Registry status
NA
Development phase
15
Enrollment target

NCT03249454: Completed NA study, sponsored by The University of Texas Health Science Center, Houston.

NCT03249454 is a NA study that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 15 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

NCT03249454, a NA study, has completed, sponsored by The University of Texas Health Science Center, Houston.

COMPLETED
Registry status
NA
Development phase
15 participants
Enrollment target

Study Summary

The purpose of the study is to investigate the effects of a novel therapeutic approach with transcutaneous spinal direct current stimulation (tsDCS) to promote functional recovery and spasticity in chronic spinal cord injury (SCI).

Primary Outcome

Immediately before application of tsDCS and after application of tsDCS, Hmax will be obtained from soleus muscle by stimulation of tibial nerve. The H-reflex is a compound muscle action potential elicited by low-threshold electrical stimulation of afferent fibers in the mixed nerve with subsequent monosynaptic excitation of alpha motoneurons. Changes in the excitability of the reflex pathway are estimated by measuring the amplitude of the reflex.

Interventions

  • DEVICE Anodal tsDCS
  • DEVICE Cathodal tsDCS
  • DEVICE Sham tsDCS

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2017-08-11
Est. Completion 2018-10-26
Phase NA

What the finished NCT03249454 record still lists

NCT03249454 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 15 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 3 interventions - of which Anodal tsDCS is the first listed.

NCT03249454 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03249454 about?

NCT03249454 is a clinical study titled "Effects of Transcutaneous Spinal Direct Current Stimulation in Incomplete Spinal Cord Injury". The purpose of the study is to investigate the effects of a novel therapeutic approach with transcutaneous spinal direct current stimulation (tsDCS) to promote functional recovery and spasticity in chronic spinal cord injury (SCI).

What is the current status of trial NCT03249454?

This trial is currently completed. It is a NA study. The enrollment target is 15 participants. The study started on 2017-08-11. Estimated completion is 2018-10-26.

What interventions are being tested in trial NCT03249454?

The interventions under investigation include: Anodal tsDCS (DEVICE), Cathodal tsDCS (DEVICE), Sham tsDCS (DEVICE).

Who is sponsoring clinical trial NCT03249454?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03249454's enrollment target sits among peer trials

15 1881st of 2000 higher than 92 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 NCT03249454, the US trial registry maintained by the National Library of Medicine. NCT03249454 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.