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Study identifier: NCT07502599 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Fainting Detection And Early Warning In Syncope Evaluation Study (ARISE)

Condition: Orthostatic Hypotension · Reflex Syncope  ·  Sponsor: Boston Scientific Corporation

PhaseN/A
Planned participants40
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

To characterize the impact of orthostatic hypotension (OH) and Vasovagal syncope on signals measured using a wearable Holter monitor in the clinic and ambulatory setting. To evaluate the relationship of signals measured from the Holter monitor with reported symptom severity of orthostatic intolerance per standard data collection, analysis, and questionnaires.

This description comes directly from the study's public registry record.

Talk to the study team

Ashley M Jensen, Masters of Science  ·  612-449-2918  ·  ashley.jensen@bsci.com

Mojgan Goftari, PhD  ·  mojgan.goftari@bsci.com

Always discuss trial participation with your own doctor first.

Locations (1)

Mayo Clinic FoundationRochester, Minnesota, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07502599