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Data Collection - Of Syncope Tilt Table Testing Study

NCT03721393 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2023-08-02

No results posted yet for this study

Summary

To characterize the impact of orthostatic hypotension (OH) and reflex syncope on signals measured using a wearable cardiac monitor prototype device.

To evaluate the relationship of signals measured from the wearable cardiac monitor prototype device with reported symptom severity of orthostatic intolerance per standard data collection, analysis, and questionnaires.

Conditions

  • Orthostatic Hypotension
  • Reflex Syncope

Interventions

DEVICE

Wearable heart monitor

Participants will be fitted with a wearable heart monitor placed on the skin that measures physiologic signals. There is no intervention or treatment.

Sponsors & Collaborators

  • Boston Scientific Corporation

    lead INDUSTRY

Principal Investigators

  • Wolfgang Singer, MD · Mayo Clinic

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-10-04
Primary Completion
2023-05-08
Completion
2023-05-08

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03721393 on ClinicalTrials.gov