Not Invasive Monitoring at Cardiac Recompensation

NCT ID: NCT01775306

Last Updated: 2014-01-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

49 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-10-31

Study Completion Date

2013-05-31

Brief Summary

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The aim of this study is to find out if data can be provided by external sensor technology which is suitable for controlling the therapy of patients with cardiac recompensation.

Detailed Description

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Conditions

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Cardiac Recompensation

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* patients with acute or chronic cardiac decompensation with and without pulmonary oedema
* male and female patients aged at least 18 years

Exclusion Criteria

* pregnancy or breast feeding
* implanted pacemaker / CRT / ICD exept Medtronic OptiVol
* patients being unable to consent
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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RWTH Aachen University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Univeristy Hospital Aachen

Aachen, North Rhine Westfalia, Germany

Site Status

Countries

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Germany

Other Identifiers

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10-081

Identifier Type: -

Identifier Source: org_study_id

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