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Not Yet Recruiting
NCT07686302
Feasibility of Noninvasive Trigeminal Nerve Stimulation During Exercise
Conditions: COPD
Sex: All
Ages: 18 Years – 75 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 40
Sponsor: Johns Hopkins University
Summary
The purpose of this study is to examine 1) effects of cutaneous electrical trigeminal nerve stimulation (eTNS) on respiratory control in healthy volunteers and 2) explore the potential of this approach to mitigate dyspnea in patients with chronic obstructive lung disease (COPD).
Eligibility Criteria
Arm1 - Healthy Volunteers
Inclusion Criteria:
* Adults aged 18-50 years
* BMI 18-30 kg/m²
* Ability to provide informed consent and complete study procedures in English
Exclusion Criteria:
* Current daytime respiratory impairment such as uncontrolled asthma, uncontrolled COPD, pneumonia, or interstitial lung disease
* Use of supplemental oxygen
* Pregnancy or breastfeeding
* Current use of acetazolamide, Sodium-glucose cotransporter-2 (SGLT2) inhibitors, or daily opioids
* History of claustrophobia or panic disorder
* Metallic implants in the craniofacial or cervical region that may interfere with electrode placement or electrical stimulation
* Implanted cardiac or neuroelectric device (e.g., pacemaker, implantable cardioverter-defibrillator (ICD), deep brain stimulator, vagus nerve stimulator, implanted drug pump)
* Open, broken, inflamed, infected, or healing skin lesions at or near facial electrode placement sites
* Resting heart rate \
Source: ClinicalTrials.gov (NCT07686302). StuddyBuddy aggregates publicly available trial information.