Clinical Trials Directory

Trials / Completed

CompletedNCT03186833

The Heart Failure With Preserved Ejection Fraction (HFpEF) Pathophysiology Study.

The Heart Failure With Preserved Ejection Fraction (HFpEF) Pathophysiology Study. Does Ageing Coupled With Vascular Effects of Comorbidities Lead to HFpEF? An In-depth Understanding From a Tertiary Centre

Status
Completed
Phase
Study type
Observational
Enrollment
85 (actual)
Sponsor
University Hospitals Coventry and Warwickshire NHS Trust · Academic / Other
Sex
All
Age
70 Years
Healthy volunteers
Accepted

Summary

The study addresses the hypothesis that a gradual build-up in arterial resistance and microvascular endothelial dysfunction due to common comorbidities such as hypertension and diabetes mellitus, on top of age related vascular and cardiac changes (mainly fibrosis and hypertrophy), is responsible for HFpEF. The HFpEF syndrome is commonly seen in elderly subjects (often females) with hypertension and diabetes. The investigators will investigate the vascular function, cardiovascular performance and myocardial fibrosis in different cohorts of subjects to try and prove this hypothesis. There will be 5 groups of subjects, all ≥ 70 years of age, as follows: A) Normal healthy volunteers without major comorbidities including hypertension or diabetes B) Patients with hypertension only (without diabetes mellitus) C) Patients with hypertension AND diabetes mellitus D) Patients with HFpEF. E) A parallel group of patients with Heart Failure with reduced Ejection Fraction (HFrEF) group. Arterial resistance measured by pulse wave velocity will be the primary measure and will be compared between groups A to D. A separate comparison will be made between groups D and E. Other secondary measures will focus on endothelial function (Laser Doppler measurements) and other cardiovascular performance measures (peak VO2 by CPEX, 6-minute walk distance). Bloods samples will be taken for NT-proBNP, high sensitivity Troponin T, Galectin 3 and also stored for testing later for vascular biomarkers.

Detailed description

The study will be a pathophysiological, single-centre, observational study, in which all 4 groups, including the parallel-group will be investigated in terms of qualitative-, echocardiographic-, arterial resistance, exercise testing (CPEX and 6-MWT), endothelial dysfunction assessment by Laser Doppler and vascular biomarker measurements. We intend to investigate if there is increasing arterial resistance from group "A" to group "D" and a significant difference in arterial resistance between groups "D" and "E" by measuring the PWV. Primary Outcome Our primary outcome will be a difference in arterial resistance between the groups and the parallel group, as measured by aortic PWV. Secondary Outcomes The secondary outcomes are to assess and compare endothelial function and cardiovascular performance in all groups as measured by the following: * Blood tests: NTproBNP, Galectin-3 * Urinalysis: Albumin, Creatinine and Metabolite profiles ("metabolomics"), related to cardiovascular risk and insulin resistance * Transthoracic echocardiography (TTE) indices of LV diastolic function, tissue Doppler imaging and strain rate imaging * Exercise tolerance: 6-minute walk test and a Cardiopulmonary Exercise Test (CPEX) * Microvascular function: Laser Doppler

Conditions

Interventions

TypeNameDescription
OTHERno interventionno intervention

Timeline

Start date
2017-06-06
Primary completion
2018-12-31
Completion
2018-12-31
First posted
2017-06-14
Last updated
2019-09-27

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT03186833. Inclusion in this directory is not an endorsement.