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Not yet recruiting Phase 1 Interventional

TEA Synchronized With Natural Breathing for EPS

ClinicalTrials.gov ID: NCT07917598

Public ClinicalTrials.gov record NCT07917598. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 5, 2026, 10:28 AM EST

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Official title

Transcutaneous Electrical Acustimulation Synchronized With Natural Breathing for Epigastric Pain Syndrome

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The goal of this study is to assess the acceptance and usability as well as safety of the AutoSTEA device is in treating epigastric pain syndrome in adults. It will also explore preliminary clinical and mechanistic signals. The main questions it aims to answer are: * Does the AutoSTEA device ease epigastric pain symptoms? * Is the AutoSTEA device safe and feasible for patients to use at their home? Participants will: * Use the device for 30-60 minutes at home each day for 4 weeks * Have a phone check-in four times through the trial (once a week). * Answer the daily and weekly questionnaires which consist of questions regarding symptoms, device usability, and adverse events experienced.

Study identification

NCT ID
NCT07917598
Recruitment status
Not yet recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
MetroHealth Medical Center
Other
Enrollment
40 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 1, 2027 (Estimated)
Primary completion
Jan 1, 2030 (Estimated)
Completion
Jul 1, 2030 (Estimated)
Last update posted
Nov 4, 2026

2027 – 2030

United States locations

U.S. sites
2
U.S. states
1
U.S. cities
2
Facility City State ZIP Site status
MetroHealth Medical Center Cleveland Ohio 44109 —
MetroHealth Parma Medical Center Parma Ohio 44130 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07917598, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 4, 2026 · Synced Nov 5, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07917598 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →