CONGEST-HF EX
Research type
Research Study
Full title
Correlation of the non-invasive Cardiopulmonary Management (CPM) wearable device with measures of congestion in heart failure in Exercise
IRAS ID
323853
Contact name
Pardeep Jhund
Contact email
Sponsor organisation
University of Glasgow
Clinicaltrials.gov Identifier
Duration of Study in the UK
1 years, 10 months, 31 days
Research summary
Heart Failure is associated with frequent and lengthy hospitalisations. These hospitalisations are usually as a result of congestion. The signs of congestion that can be recognised by physicians or health care professionals such as lung crackles or worsening of peripheral oedema are often seen at a late stage before an intervention can be made to prevent overt decompensation and admission to hospital. Recognising changes in excess fluid status either before a patient becomes unwell or during decongestion treatment is highly desirable so that timely treatment can be started or so that treatment can be adjusted based on an individual's response to therapy. The ability to assess patients by applying a single, non-invasive device would potentially provide a useful tool for assessing a patient’s congestion levels and allow patients with progressive deterioration to be identified earlier.
REC name
London - Dulwich Research Ethics Committee
REC reference
23/LO/0207
Date of REC Opinion
15 Mar 2023
REC opinion
Favourable Opinion