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TRAnscranial Doppler CErebral Blood Flow and Cognitive IMPAIRment in Heart Failure

TRAnscranial Doppler CErebral Blood Flow and Cognitive IMPAIRment in Patients With Heart Failure and Presence/Absence of Atherosclerotic Carotid Artery Stenosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05250349
Acronym
TRACE-IMPAIR
Enrollment
300
Registered
2022-02-22
Start date
2021-09-01
Completion date
2027-09-01
Last updated
2022-02-22

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

Conditions

Carotid Stenosis, Cognitive Impairment, Heart Failure

Keywords

Carotid Stenosis, Heart Failure, Carotid Doppler, Transcranial Doppler, Cerebral Flow, Cognitive Impairment, Stroke Volume

Brief summary

TRACE-IMPAIR is a prospective, clinical study of consecutive patients that evaluates the relationship between heart failure (HF) and cognitive impairment in relation to carotid and cerebral flow. The carotid and cerebral flow will be assessed using Doppler ultrasonography, and cognitive function will be estimated during routine neuropsychological tests. It is an observational, three(natural)-group, single-center study. It is also an Academic Registry - the scientific activity of the Faculty of Medicine, Collegium Medicum, Jagiellonian University, and John Paul II Hospital.

Detailed description

Circumstantial evidence suggests that cognitive dysfunction may occur in HF patients as often undiagnosed comorbidity. Cognitive dysfunction may aggravate HF symptoms and influence prognosis. Cognitive dysfunction may be a reason for inadequate self-care and poor symptom control (e.g., weight gain monitoring). In addition, it may affect medication compliance, leading to hospital readmissions and increased mortality. Brain tissue hypoxia, microemboli, silent strokes, and co-existing anemia have been implicated in contributing to cognitive dysfunction in HF. However, the role of cerebral flow impairment in these patients remains unclear. This uncertainty is mainly because previous studies included small patient groups, diverse imaging techniques, and neuropsychological tests. Furthermore, these studies were primarily conducted in the elderly, a potentially important confounder due to the effect of age on cognitive dysfunction. Particularly little data is available for younger patients (\< 60 years). This study aims to investigate the association of HF, carotid and cerebral flow, and cognitive impairment. Consecutive patients with HF with mildly reduced (HFmrEF) and reduced ejection fraction (HFrEF) will be included in the study. Echocardiography with routine measurements such as ejection fraction and stroke volume will be performed in each patient. The carotid and cerebral flow will be assessed on Doppler ultrasonography. Each patient will undergo cognitive function assessment using Mini-Mental State Examination (MMSE) and Montreal Cognitive Assessment (MoCA). The results in the index group (isolated HF) will be compared with those in a group of patients with HF and flow-limiting carotid stenosis (CS) against a control group (no HF, no CS).

Interventions

DIAGNOSTIC_TESTEchocardiography

Transthoracic echocardiography with standard measurements

DIAGNOSTIC_TESTDoppler sonography

Transcarotid and transcranial Doppler sonography

DIAGNOSTIC_TESTNeuropsychological tests

Mini Mental State Examination (MMSE) and Montreal Cognitive Assessment (MoCA)

Sponsors

John Paul II Hospital, Krakow
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Clinically stable patients (NYHA I-III symptoms) with HF (for at least 6 months) either of ischemic or inflammatory etiology as well as genetic cardiomyopathies * Signed informed consent form * Consent to imaging studies: echocardiography, carotid and transcranial Doppler sonography and neuropsychological tests (MMSE and MoCA).

Exclusion criteria

* Co-existing, severe, irreversible disease (e.g. advanced cancer) * Previously diagnosed dementia (including severe dementia - MMSE and MoCA score \<10) * Psychiatric condition which may influence cognitive function * Acute, decompensated HF * Reversible cause of HF - tachyarrhytmic, peripartum or toxic cardiomyopathy, acute myocarditis, acute myocardial infarction * Aortic stenosis * Cerebral stroke in the preceding 3 months * Lack of transcranial Doppler acoustic window * Echocardiographic projections precluding adequate measurements * Anemia with Hemoglobin \< 8 g/dl * Alcohol or psychoactive agents abuse

Design outcomes

Primary

MeasureTime frameDescription
Proportion of patients with at least moderate (i.e. mild or moderate) cognitive dysfunction (MMSE)At six months from HF diagnosisProportion of patients with at least moderate (i.e. mild or moderate) cognitive dysfunction according to Mini Mental State Examination (MMSE score ≥10)

Secondary

MeasureTime frameDescription
Proportion of patients with mild cognitive dysfunction (MMSE)At six months from HF diagnosisProportion of patients with mild cognitive dysfunction according to Mini Mental State Examination (MMSE score 20 - 25)
Proportion of patients with mild cognitive dysfunction (MoCA)At six months from HF diagnosisProportion of patients with mild cognitive dysfunction according to Montreal Cognitive Assessment (MoCA score 18 - 25)
Proportion of patients with moderate cognitive dysfunction (MMSE)At six months from HF diagnosisProportion of patients with moderate cognitive dysfunction according to Mini Mental State Examination (MMSE score 10 - 19)4. Proportion of patients with moderate cognitive dysfunction according to Mini Mental State Examination (MMSE score 10 - 19)
Proportion of patients with at least moderate (i.e. mild or moderate) cognitive dysfunction (MoCA)At six months from HF diagnosisProportion of patients with at least moderate (i.e. mild or moderate) cognitive dysfunction according to Montreal Cognitive Assessment (MoCA score ≥10)
Proportion of patients with moderate reduced cerebral flow velocityAt six months from HF diagnosisProportion of patients with reduced cerebral flow velocity (mean cerebral flow velocity \<50 cm/s) in the middle cerebral artery among those with at least moderate (i.e. mild or moderate) cognitive dysfunction according to MMSE (MMSE score ≥10)
Proportion of patients with significantly reduced cerebral flow velocityAt six months from HF diagnosisProportion of patients with reduced cerebral flow velocity (mean cerebral flow velocity \<50 cm/s) in the middle cerebral artery among those with at least moderate (i.e. mild or moderate) cognitive dysfunction according to MoCA tests (MoCA score≥10)
Proportion of patients with moderate cognitive dysfunction (MoCA)At six months from HF diagnosisProportion of patients with moderate cognitive dysfunction according to Montreal Cognitive Assessment (MoCA score 10 - 17)

Countries

Poland

Contacts

Primary ContactPiotr Musialek, MD, DPhil
pmusialek@szpitaljp2.krakow.pl+48126142287
Backup ContactKarolina Dzierwa, MD, PhD
kdzierwa@szpitaljp2.krakow.pl+48126143158

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026