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Study of the Relationships Between Refractory Hypertension, Overweight/Obesity and Sleep Apnea Syndrome (RHOOSAS)

Primary Purpose

Refractory Hypertension

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
nCPAP
Sponsored by
University Hospital, Grenoble
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Refractory Hypertension focused on measuring Refractory hypertension, Obstructive sleep apnea syndrome, Obesity, Leptinemia, RHOOSAS study

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients of either gender, of between 18 and 70
  • Suffering from refractory hypertension as defined by persistent clinical hypertension (> 140/90 mm Hg according to two different readings 24 hours apart) despite at least three classes of antihypertensive drugs (including a thiazide diuretic) at appropriate doses.
  • Recruited in the Cardiology Departments of the University Hospitals in Grenoble, Toulouse, Marseille and Poitiers, and in the Mozart Clinic in Paris.
  • Outpatients
  • Patients who have signed the consent form
  • Patients affiliated to or beneficiary of the social security system

Exclusion Criteria:

  • Failure to fulfil the inclusion criteria
  • Treated SAS, whatever the form of the treatment
  • Disease which might affect BP regulation, including Parkinson's disease, kidney or heart transplantation, dysautonomia, severe heart failure
  • Atrial fibrillation or regular extrasystole (> 10/minute)
  • Night- or shift-work
  • Pregnant and breast-feeding women
  • Patients under legal guardianship
  • Incarcerated patients or adults protected by the law
  • Hospitalised patients
  • Ongoing participation in another clinical research study

Sites / Locations

  • University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

1

2

Arm Description

Arm 1: Active CPAP, a nasal continuous positive airway pressure

Arm 2 : Sham CPAP :Placebo/CPAP

Outcomes

Primary Outcome Measures

leptinemia

Secondary Outcome Measures

BP readings (clinical and ABPM), metabolic parameters (lipids, glycaemia, adiponectin) and sympathetic nervous system effectors (adrenaline, noradrenaline and metanephrines).

Full Information

First Posted
September 3, 2008
Last Updated
November 6, 2014
Sponsor
University Hospital, Grenoble
Collaborators
Fondation de Recherche sur l'Hypertension Artérielle
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1. Study Identification

Unique Protocol Identification Number
NCT00746902
Brief Title
Study of the Relationships Between Refractory Hypertension, Overweight/Obesity and Sleep Apnea Syndrome
Acronym
RHOOSAS
Official Title
Study of the Relationships Between Refractory Hypertension, Overweight/Obesity and Sleep Apnea Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
November 2014
Overall Recruitment Status
Completed
Study Start Date
June 2008 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
September 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Grenoble
Collaborators
Fondation de Recherche sur l'Hypertension Artérielle

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to investigate the links between blood pressure (BP), overweight or obesity, and sleep apnea syndrome (SAS), by studying a large cohort of subjects suffering from refractory hypertension. Primary objective To compare plasmatic leptin levels in patients suffering from refractory hypertension depending on whether or not they experience SAS. Secondary objectives To ascertain what determines the difference in plasmatic leptin concentrations in patients suffering from refractory hypertension depending on whether or not they experience SAS. To characterise BP readings (from clinical and ambulatory (ABPM) measurements) in patients suffering from refractory hypertension depending on whether or not they experience SAS. To characterise metabolic parameters (lipids, glycaemia, adiponectin) and sympathetic nervous system effectors (adrenaline, noradrenaline and metanephrines) in patients suffering from refractory hypertension depending on whether or not they experience SAS. To characterise BP readings, metabolic parameters and sympathetic nervous system effectors in patients suffering from refractory hypertension according to the severity of the SAS (in those who experience this problem). To study, in patients with both SAS and refractory hypertension, the impact of nasal continuous positive airway pressure (CPAP) treatment on BP readings, metabolic parameters and sympathetic nervous system effectors, by comparing those who are compliant with the CPAP regimen with those who are non-compliant.
Detailed Description
A number of factors predispose subjects to both hypertension and SAS, including overweight/obesity and hyperinsulinism. The pathogenesis of concomitant overweight/obesity and hypertension is multifactorial. There is an independent relationship between the degree of insulin resistance and the severity of SAS. A number of studies have suggested that hormones secreted by adipose tissue are involved in the pathogenesis of both hypertension and SAS, and overweight/obesity has been shown to be associated with elevated leptin levels coupled with reduced adiponectin levels. Leptin is produced in adipose tissue and its levels rise with overweight/obesity due to peripheral resistance to its action. A number of studies have detected high leptinemia in both hypertensives and people suffering from SAS. Leptin may activate the sympathetic nervous system and promote SAS-related hypertension. Adiponectin which is also produced in adipose tissue has beneficial activities, notably on atherogenesis. A relationship between hypertension and adiponectin has yet to be demonstrated. Unlike leptin, adiponectin levels do not seem to be elevated in patients with SAS. In terms of treatment, a number of studies have shown that CPAP has a positive effect on BP readings. Although this effect is modest, it is greater in subjects with SAS and rises with the severity of this condition. The effects of CPAP on plasmatic leptin and adiponectin levels are as yet unknown.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Refractory Hypertension
Keywords
Refractory hypertension, Obstructive sleep apnea syndrome, Obesity, Leptinemia, RHOOSAS study

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
62 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Arm 1: Active CPAP, a nasal continuous positive airway pressure
Arm Title
2
Arm Type
Sham Comparator
Arm Description
Arm 2 : Sham CPAP :Placebo/CPAP
Intervention Type
Device
Intervention Name(s)
nCPAP
Intervention Description
Active nCPAP
Primary Outcome Measure Information:
Title
leptinemia
Time Frame
inclusion visit, visit month 3, visit month 6 or 9
Secondary Outcome Measure Information:
Title
BP readings (clinical and ABPM), metabolic parameters (lipids, glycaemia, adiponectin) and sympathetic nervous system effectors (adrenaline, noradrenaline and metanephrines).
Time Frame
inclusion visit, visit month 3, visit month 6 or 9

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients of either gender, of between 18 and 70 Suffering from refractory hypertension as defined by persistent clinical hypertension (> 140/90 mm Hg according to two different readings 24 hours apart) despite at least three classes of antihypertensive drugs (including a thiazide diuretic) at appropriate doses. Recruited in the Cardiology Departments of the University Hospitals in Grenoble, Toulouse, Marseille and Poitiers, and in the Mozart Clinic in Paris. Outpatients Patients who have signed the consent form Patients affiliated to or beneficiary of the social security system Exclusion Criteria: Failure to fulfil the inclusion criteria Treated SAS, whatever the form of the treatment Disease which might affect BP regulation, including Parkinson's disease, kidney or heart transplantation, dysautonomia, severe heart failure Atrial fibrillation or regular extrasystole (> 10/minute) Night- or shift-work Pregnant and breast-feeding women Patients under legal guardianship Incarcerated patients or adults protected by the law Hospitalised patients Ongoing participation in another clinical research study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Philippe BAGUET, Professor
Organizational Affiliation
University Hospital, Grenoble
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital
City
Grenoble
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
29867728
Citation
Joyeux-Faure M, Baguet JP, Barone-Rochette G, Faure P, Sosner P, Mounier-Vehier C, Levy P, Tamisier R, Pepin JL. Continuous Positive Airway Pressure Reduces Night-Time Blood Pressure and Heart Rate in Patients With Obstructive Sleep Apnea and Resistant Hypertension: The RHOOSAS Randomized Controlled Trial. Front Neurol. 2018 May 8;9:318. doi: 10.3389/fneur.2018.00318. eCollection 2018.
Results Reference
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Study of the Relationships Between Refractory Hypertension, Overweight/Obesity and Sleep Apnea Syndrome

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