Not Invasive Monitoring at Cardiac Recompensation

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01775306

Enrollment

Registered

2013-01-24

Start date

2011-10-31

Completion date

2013-05-31

Last updated

2014-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Recompensation

Brief summary

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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 90 Years

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

Design outcomes

Primary

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

Countries

Germany

Outcome results