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Clinical Trials/NCT05845736
NCT05845736
Completed
Not Applicable

The Impact of Dementia and Neurocognitive Disorders on Hypertension Treatment in the Very Elderly: the TAHOC Study

Central Hospital, Nancy, France1 site in 1 country353 target enrollmentJanuary 1, 2022

Overview

Phase
Not Applicable
Intervention
Antihypertensive Agents
Conditions
Neurocognitive Disorders
Sponsor
Central Hospital, Nancy, France
Enrollment
353
Locations
1
Primary Endpoint
number of antihypertensive agents
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Neurocognitive disorders and hypertension occur commonly with aging. While, by definition, older adults are at high cardiovascular risk, there is no guideline exist currently on blood pressure management of elderly hypertension. However, studies have shown that in aging adults, high blood pressure helps prevent against cognitive decline, and low blood pressure on antihypertensive drugs could accelerate it. This study aims at investigating if pharmacological treatment of hypertension in the very elderly is influenced by presence and severity of neurocognitive disorders. Our research hypothesis is that the drug management of hypertension in patients 80 years of age or older more is all the less aggressive as the neurocognitive disorders are advanced.

Registry
clinicaltrials.gov
Start Date
January 1, 2022
End Date
December 12, 2022
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Central Hospital, Nancy, France
Responsible Party
Principal Investigator
Principal Investigator

Pr Athanase BENETOS

principal investigator

Central Hospital, Nancy, France

Eligibility Criteria

Inclusion Criteria

  • to be 80 years of age
  • with history of hypertension and/or on hypertensive drug(s)

Exclusion Criteria

  • legal protection measure.

Arms & Interventions

control group

absence of neurocognitive disorder (ND), Mini-Mental State Examination (MMSE) from 27 to 30 inclusive

Intervention: Antihypertensive Agents

mild neurocognitive disorder

MMSE from 21 to 26 inclusive

Intervention: Antihypertensive Agents

moderate neurocognitive disorder

MMSE from 11 to 20 inclusive

Intervention: Antihypertensive Agents

severe neurocognitive disorder

MMSE less than or equal to 10

Intervention: Antihypertensive Agents

Outcomes

Primary Outcomes

number of antihypertensive agents

Time Frame: during inclusion

among ACEI/ARB2, calcium channel blocker, thiazides and related, central antihypertensive beta blocker

Secondary Outcomes

  • orthostatic hypotension(during inclusion)
  • class of antihypertensive medications(during inclusion)
  • systolic and diastolic blood pressure(during inclusion)

Study Sites (1)

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