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Breathing Rescue for SUDEP Prevention

Breathing Rescue for SUDEP Prevention (BreatheS)

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05981755
Acronym
BreatheS
Enrollment
100
Registered
2023-08-08
Start date
2023-07-31
Completion date
2028-06-30
Last updated
2025-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Focal Epilepsy

Brief summary

The purpose of this study is to precisely delineate human brain networks that modulate respiration and identify specific brain areas and stimulation techniques that can be used to prevent seizure-induced breathing failure.

Interventions

OTHERBreathing tasks

Breathing tasks include normal breathing through nose or mouth, breathing while resting wakefully, increase and decrease in breathing rate, and breath counting.

DEVICEBrain mapping with stimulation

Electrical stimulation will be used to find specific areas of the brain involved in breathing function. Stimulation will be applied using a Nihon Kohden MEE-1000A neural function measuring system with the MS-120BK extension unit for brain stimulation.

Sponsors

National Institute of Neurological Disorders and Stroke (NINDS)
CollaboratorNIH
The University of Texas Health Science Center, Houston
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* diagnosis of intractable focal epilepsy * admitted to the Epilepsy Monitoring Unit (EMU) at Memorial Hermann-Texas Medical Center for intracranial subdural strips, grids, or depth electrode placement study (invasive video-EEG)

Exclusion criteria

* respiratory, cardiac or cerebrovascular disease * pregnancy * prisoners

Design outcomes

Primary

MeasureTime frameDescription
Change in end tidal carbon dioxide (CO2) during stimulationBaseline, during the stimulation session (at least 2 hours after baseline)Lower and higher frequencies up to 50Hz, current of 1-10mA, pulse durations of 0.2 msec and stimulation periods of 10 to 40 seconds will be used.
Changes in thoracoabdominal circumference during stimulation as assessed by thoracoabdominal belts,Baseline, during the stimulation session (at least 2 hours after baseline)Lower and higher frequencies up to 50 Hertz(Hz), current of 1-10 milli ampere (mA), pulse durations of 0.2 milli second (msec) and stimulation periods of 10 to 40 seconds will be used.
Changes airflow during stimulation as assessed by the nasal/oral pressure transducer [BiNAPS]Baseline, during the stimulation session (at least 2 hours after baseline)Lower and higher frequencies up to 50Hz, current of 1-10mA, pulse durations of 0.2 msec and stimulation periods of 10 to 40 seconds will be used.
Change in Saturation of peripheral oxygen (SpO2) during stimulation as assessed by the pulse oximetryBaseline, during the stimulation session (at least 2 hours after baseline)Lower and higher frequencies up to 50Hz, current of 1-10mA, pulse durations of 0.2 msec and stimulation periods of 10 to 40 seconds will be used.
Change in percentage of breathing node size as assessed by electroencephalogram (EEG) signalbaseline (before breathing task), at the time of the breathing task (about 8 minutes after start of baseline)
Change in presence of breathing nodes as assessed by EEG signalBaseline (before breathing task), at the time of the breathing task(about 8 minutes after start of baseline)

Secondary

MeasureTime frameDescription
Quantification of the breathing changes as assessed by the change in breathing depthbaseline (before stimulation), at the time of stimulation (about 8 minutes after start of baseline)Breathing depth, or tidal volume (TV), is the amount of air that normally enters the lungs during quiet breathing. Breathing changes will be visually identified live during stimulation sessions using thoraco-abdominal plethysmography and pressure transducer signal (nasal/oral airflow).
Quantification of the breathing changes as assessed by the change in breathing minute ventilation (MV)baseline (before stimulation), at the time of stimulation (about 8 minutes after start of baseline)Minute ventilation, also known as total ventilation, is a measurement of the amount of air that enters the lungs per minute. It is the product of respiratory rate and tidal volume. Breathing changes will be visually identified live during stimulation sessions using thoraco-abdominal plethysmography and pressure transducer signal (nasal/oral airflow).
Quantification of the breathing changes as assessed by the change in breathing ratebaseline (before stimulation), at the time of stimulation (about 8 minutes after start of baseline)Breathing rate is the number of breaths taken per minute. Breathing changes will be visually identified live during stimulation sessions using thoraco-abdominal plethysmography and pressure transducer signal (nasal/oral airflow).

Countries

United States

Contacts

Primary ContactNuria L Lecumberri, MD,PhD
Nuria.Lacuey@uth.tmc.edu713-500-7785
Backup ContactSandhya Rani, PhD
M.R.Sandhya.Rani@uth.tmc.edu713-500-7499

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026