Not Invasive Monitoring at Cardiac Recompensation

R

RWTH Aachen University

Status

Completed

Conditions

Cardiac Recompensation

Study type

Observational

Funder types

Other

Identifiers

NCT01775306
10-081

Details and patient eligibility

About

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.

Enrollment

49 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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