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Proof of Concept Study for 1 Lead Patch Technology

NCT02533531 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1

Last updated 2018-04-06

Study results available
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Summary

This study is intended to assess the feasibility and usability of the 1 Lead Patch as a whole, on patients outside the hospital, in the out-patient setting.

Conditions

  • Telemetry

Interventions

DEVICE

1-Lead Patch

The 1-Lead Patch will record and transmit ECG data to a gateway, which will then transmit the data to a central database.

Sponsors & Collaborators

  • LifeWatch Services, Inc.

    lead INDUSTRY

Principal Investigators

  • Vivek Reddy, MD FACC FHRS · Mt. Sinai Medical Center

  • Marie Noelle-Langan, MD · Mt. Sinai Medical Center

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-04-16
Primary Completion
2016-06-09
Completion
2016-06-09
FDA Device
Yes

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 NCT02533531 on ClinicalTrials.gov