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Spinal zap + breathing drills may restore lung power after paralysis

NCT ID NCT05178056

Symptom relief Sponsor: University of Louisville Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether a spinal cord stimulator, combined with breathing exercises, can improve respiratory function in people with chronic spinal cord injury. Thirty adults with neck-level injuries will undergo 16 weeks of training while using the device. Researchers will measure changes in breathing strength and muscle activity to see if this combination works better than training alone.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Spinal cord epidural stimulation device
What this could lead to
If successful, this could lead to a new rehabilitation approach that helps people with spinal cord injury breathe more easily and reduce related health risks.
What could go wrong
This is an early-stage study with only 30 participants, so results may not apply to everyone. The device requires surgery, which carries risks like infection or device complications.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 30 people

The number the study aims to enrol. It can still change while the study runs.

Started

Dec 2021

Expected to finish

Dec 2030

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * At least 18 years old * Stable medical condition * Non-progressive C3-T1 AIS A-C Spinal Cord Injury (SCI) * Sustained SCI at least 24 months prior to entering the study * At least 15%-deficit in pulmonary function outcomes Exclusion Criteria: * Painful musculo-skeletal dysfunction * Unhealed fracture * Contracture * Pressure sore * Urinary tract infection that might interfere with respiratory training * Clinically significant depression * Psychiatric disorders * Ongoing drug abuse; * Major cardiovascular disease * Major pulmonary disease * Ventilator dependence * Major endocrine disorders * Malignancy * Marked obesity * Deep vein thrombosis * HIV/AIDS related illness * Secondary causes of respiratory dysfunction * Major gastrointestinal problems * Other major medical illness contraindicated for respiratory training * Pregnantcy

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Conditions

The condition(s) this trial relates to.

spinal cord injury

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Breathing exercises Rehabilitation Spinal cord injuries Spinal cord stimulation

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Frazier Rehabilitation and Neuroscience Institute

    RECRUITING

    Louisville, Kentucky, 40202, United States

More trials for these conditions

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