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Acute Congestive Heart Failure

NCT01885403 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2015-09-23

No results posted yet for this study

Summary

The aim of the study is to determine the feasibility of collecting respiratory parameters during recompensation following ADHF (Acute Decompensated Heart Failure)with non-invasive measurements. This could lead to a better understanding of how respiratory parameters may change during re-compensation therapy and could also be a comfortable method for patients.

Conditions

  • Acute Decompensated Heart Failure (ADHF)
  • Acute Cardiogenic Pulmonary Edema (ACPE)

Interventions

DEVICE

non-invasive respiratory parameter measurements

Sponsors & Collaborators

  • Philips Technology Aachen Germany

    collaborator UNKNOWN

  • RWTH Aachen University

    lead OTHER

Principal Investigators

  • Jörg Schröder, MD · Department of Cardiology, Pneumology, Angiology and Intensive Care, Internal Medicine I (MK I), University Hospital Aachen (UKA)

Study Design

Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-06-30
Primary Completion
2015-12-31
Completion
2016-04-30

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01885403 on ClinicalTrials.gov