Not Invasive Monitoring at Cardiac Recompensation

RWTH Aachen University49 enrolled

Overview

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.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Cardiac Recompensation

Eligibility

Sex: ALLMin age: 18 YearsMax age: 90 Years

Medical Language ↔ Plain English

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

Locations (1)

Univeristy Hospital Aachen

Aachen, North Rhine Westfalia, Germany

Outcomes

Primary Outcomes

suitable Data

Time frame: 15 minutes per day and per patient, 3-5 days, at most 14 days

Data from ClinicalTrials.gov

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