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CareLink Express (CLE Research)

NCT03223207 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2019-05-22

No results posted yet for this study

Summary

The primary objective of this research is to determine if evaluating CIEDs using CareLink Express® can lead to shorter time to interrogation in the Emergency Department compared to evaluation of devices using traditional evaluation procedures. The goal of the research is to determine if patients evaluated by CareLink Express® have a reduction of "time to interrogation" compared to the traditional patient cohort.

Secondary objectives of the study are to determine any significant differences in the two populations regarding:

1. Health care resource utilization including total charges for ED care.
2. Number of patients leaving the ED without being seen (LWBS) or left without the device interrogation completed.
3. Device related issues detected.

Conditions

Sponsors & Collaborators

  • Medtronic

    collaborator INDUSTRY

  • Baylor Research Institute

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-03-31
Primary Completion
2018-08-27
Completion
2018-08-27

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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 NCT03223207 on ClinicalTrials.gov