Not Invasive Monitoring at Cardiac Recompensation

Completed

• Conditions: Cardiac Recompensation

• Registration Number: NCT01775306
• Lead Sponsor: RWTH Aachen University

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2011-10
• Study First Submitted: 2013-01-22
• Study First Submitted QC: 2013-01-22
• Study First Posted: 2013-01-24
• Primary Completion: 2013-05
• Study Completion: 2013-05
• Status Verified: 2014-01
• Last Update Submitted: 2014-01-07
• Last Update Posted: 2014-01-08

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 49

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

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

Trial Locations

Locations (1)

Univeristy Hospital Aachen; 🇩🇪 Aachen, North Rhine Westfalia, Germany