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Impact of the Reduction in Antihypertensive Treatment on Total Mortality in Frail Subjects With Low Systolic Blood Pressure: Study in Subjects Over 80 Years Living in Nursing Homes (RETREAT-FRAIL)

Primary Purpose

Hypertension

Status
Active
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
STEP DOWN strategy
Control
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Hypertension focused on measuring Blood pressure, Aged, Frailty, Polypharmacy

Eligibility Criteria

80 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient 80 years or older
  • Patient living in a NH
  • SBP <130 mmHg, as measured (with an electronic device with recorder) in nursing homes by nurses (average of 3 measurements after 10 min of rest). These SBP values should be recorded in the absence of any acute illness or condition inducing acute BP drop
  • Patient treated for hypertension with 2 or more antihypertensive drugs
  • Stable antihypertensive treatment (3 weeks for an introduction or stop and 2 weeks for a posology change)
  • Mandatory enrollment in a social security plan
  • Patient (or legal representative if applicable) having signed an informed consent.

Exclusion Criteria:

  • Patient in which none of antihypertensive drugs can be stopped because of simultaneous indications for other cardiovascular diseases.
  • Patient with estimated life expectancy <3 months.
  • Patient who has already been included in this study

Sites / Locations

  • Gériatrie - CHRU de Nancy

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

1: Interventional (drug reduction)

2: Control

Arm Description

STEP DOWN strategy. Proposition of reduction of the number of antihypertensive medication according to: the systolic blood pressure levels, co-morbidities

Usual treatment

Outcomes

Primary Outcome Measures

All-cause mortality
during a follow up period of 24 months minimal to 48 months maximal

Secondary Outcome Measures

Blood pressure analysis
Systolic BP, diastolic BP, pulse pressure (PP) in sitting position and then in upright position during the follow up period of 24-48 months
Cause of deaths
Major cardiovascular (CV) events (myocardial infarction, hospitalization for heart failure, stroke and any other serious CV complications requiring specific treatment or hospitalization) during the follow up period of 24-48 months
Evaluation of frailty
assessed by muscular force and Short Physical Performance Battery every 6 months
Evaluation of autonomy
assessed by scale Activites of Daily Living scale every 6 months
Evaluation of cognitive function
assessed by Mini Mental Status Evaluation (MMSE) every 6 months
Number of falls
Number of falls and recording of fractures during the follow up period of 24-48 months
Medications
Total number of medications, number of anti-hypertensive drugs during the follow up period of 24-48 months
Evaluation of Quality of Life
Indices of Quality of Life (EQ 5D) yearly

Full Information

First Posted
January 31, 2018
Last Updated
March 10, 2023
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT03453268
Brief Title
Impact of the Reduction in Antihypertensive Treatment on Total Mortality in Frail Subjects With Low Systolic Blood Pressure: Study in Subjects Over 80 Years Living in Nursing Homes
Acronym
RETREAT-FRAIL
Official Title
Impact of the Reduction in Antihypertensive Treatment on Total Mortality in Frail Subjects With Low Systolic Blood Pressure: Randomized, Controlled Study in Subjects Over 80 Years Living in Nursing Homes
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 2, 2018 (Actual)
Primary Completion Date
July 2, 2024 (Anticipated)
Study Completion Date
July 2, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigators hypothesize that a gradual reduction in antihypertensive treatment in nursing home (NH) patients with low systolic blood pressure (SBP) can improve survival through a controlled increase in SBP and a decrease in secondary morbidity due to 'overmedication'. Accordingly, the investigators propose a randomized, case/control trial in NH patients ≥ 80 years with a SBP<130 mmHg with >1 anti-Htn drugs. This trial will consist of two parallel arms: the intervention arm will entail antihypertensive drug step-down, while the control arm will comprise the standard anti-hypertensive treatment.
Detailed Description
High blood pressure (BP), principally systolic hypertension, is a common condition in older people and is considered a major determinant not only of cardiovascular morbidity and mortality, but also of several other age-related diseases, including frailty, cognitive decline and loss of autonomy. The Hypertension in the Very Elderly Treatment (HYVET) study showed the beneficial effect of antihypertensive treatment in patients ≥ 80 years. More recently, the Systolic Blood Pressure Intervention Trial (SPRINT) study showed that even in subjects 75 years and older, CVD outcomes and total mortality were reduced with intensive treatment as compared to the standard therapeutic strategies. However, both HYVET and SPRINT were conducted in selected populations since they excluded the most frail subjects, those with clinically significant cognitive decline and dementia, those with several cardiovascular and other co-morbidities, as well as patients living in nursing homes. Interestingly, observational studies in these frail people, have shown no or even an inverse relationship between BP and morbidity and mortality. The PARTAGE longitudinal study was performed in 1130 subjects ≥ 80 years living in nursing homes (NHs). These subjects were receiving at mean 7.1 drugs/day; 2/3 of them were under antihypertensive drugs (mean 2.2 drugs/day). The PARTAGE study showed an over-mortality in hypertensive subjects with low SBP (<130 mmHg) treated with 2 or more antihypertensive drugs. These individuals, who represented 20% of the total studied population, exhibited 80% increase in mortality compared to all other groups, even after adjustment for several comorbidities. The recent European guidelines for hypertension indicate that in people ≥ 80 years with SBP≥160 mmHg there is evidence to recommend reducing SBP to between 150 and 140 mmHg. However, no recommendation exists on which strategy to follow if treatment decreases SBP to lower levels (ex: 120 mmHg) especially on the more frail and polymedicated patients of that age. Thus, in this case, physicians can either continue the same treatment of reduce the number of drugs. These contrasting results in old hypertensives reflects the enormous functional heterogeneity among individual of this age-group and clearly show that functional status rather than chronological age should guide therapeutic strategies. Thus, the guidelines for robust older individuals cannot be extrapolated to very old, frail individuals, who have been completely excluded from the above-mentioned clinical trials. The only way is to conduct a controlled clinical trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension
Keywords
Blood pressure, Aged, Frailty, Polypharmacy

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Therapeutic strategies: reduction of the antihypertensive treatment (intervention arm) vs. usual treatment (control arm)
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1126 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1: Interventional (drug reduction)
Arm Type
Other
Arm Description
STEP DOWN strategy. Proposition of reduction of the number of antihypertensive medication according to: the systolic blood pressure levels, co-morbidities
Arm Title
2: Control
Arm Type
Other
Arm Description
Usual treatment
Intervention Type
Other
Intervention Name(s)
STEP DOWN strategy
Intervention Description
reduction of the number of antihypertensive medication according to: the systolic blood pressure levels, co-morbidities
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
usual treatment
Primary Outcome Measure Information:
Title
All-cause mortality
Description
during a follow up period of 24 months minimal to 48 months maximal
Time Frame
up to 48 months
Secondary Outcome Measure Information:
Title
Blood pressure analysis
Description
Systolic BP, diastolic BP, pulse pressure (PP) in sitting position and then in upright position during the follow up period of 24-48 months
Time Frame
up to 48 months
Title
Cause of deaths
Description
Major cardiovascular (CV) events (myocardial infarction, hospitalization for heart failure, stroke and any other serious CV complications requiring specific treatment or hospitalization) during the follow up period of 24-48 months
Time Frame
up to 48 months
Title
Evaluation of frailty
Description
assessed by muscular force and Short Physical Performance Battery every 6 months
Time Frame
up to 48 months
Title
Evaluation of autonomy
Description
assessed by scale Activites of Daily Living scale every 6 months
Time Frame
up to 48 months
Title
Evaluation of cognitive function
Description
assessed by Mini Mental Status Evaluation (MMSE) every 6 months
Time Frame
up to 48 months
Title
Number of falls
Description
Number of falls and recording of fractures during the follow up period of 24-48 months
Time Frame
up to 48 months
Title
Medications
Description
Total number of medications, number of anti-hypertensive drugs during the follow up period of 24-48 months
Time Frame
up to 48 months
Title
Evaluation of Quality of Life
Description
Indices of Quality of Life (EQ 5D) yearly
Time Frame
up to 48 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient 80 years or older Patient living in a NH SBP <130 mmHg, as measured (with an electronic device with recorder) in nursing homes by nurses (average of 3 measurements after 10 min of rest). These SBP values should be recorded in the absence of any acute illness or condition inducing acute BP drop Patient treated for hypertension with 2 or more antihypertensive drugs Stable antihypertensive treatment (3 weeks for an introduction or stop and 2 weeks for a posology change) Mandatory enrollment in a social security plan Patient (or legal representative if applicable) having signed an informed consent. Exclusion Criteria: Patient in which none of antihypertensive drugs can be stopped because of simultaneous indications for other cardiovascular diseases. Patient with estimated life expectancy <3 months. Patient who has already been included in this study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Athanase BENETOS, MD, PhD
Organizational Affiliation
CHRU NANCY - Pôle Gérontologie
Official's Role
Principal Investigator
Facility Information:
Facility Name
Gériatrie - CHRU de Nancy
City
Nancy
ZIP/Postal Code
54500
Country
France

12. IPD Sharing Statement

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Impact of the Reduction in Antihypertensive Treatment on Total Mortality in Frail Subjects With Low Systolic Blood Pressure: Study in Subjects Over 80 Years Living in Nursing Homes

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