Sleep Apnea Clinical Trial
— RAPOfficial title:
Comparison of Standard Treatment by Continuous Positive Airway Pressure (CPAP) and CPAP Combined to a Physical Activity Program for Reducing Blood Pressure in Sleep Apnea Patients With Resistant Hypertension: RAP Randomized Controlled Trial
NCT number | NCT02057783 |
Other study ID # | 13-AGIR-04 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | March 26, 2015 |
Est. completion date | July 2019 |
Verified date | June 2018 |
Source | AGIR à Dom |
Contact | Jean-Louis Pépin, Pr MD PhD |
JPepin[@]chu-grenoble.fr | |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Investigators hypothesize that CPAP treatment for suppressing OSAS in combination with a physical activity program will optimize 24-hour blood pressure control in patients with OSA-related resistant hypertension.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | July 2019 |
Est. primary completion date | July 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Patient with an obstructive sleep apnea (apnea-hypopnea index > or equal to 15) - Patient with resistant hypertension uncontrolled by 3 or more antihypertensive agents - Ambulatory patient Exclusion Criteria: - Acute hepatic failure, biliary cirrhosis, cholestasis - Acute hypertension (SBP>= 180 mmHg and/or DBP >= 110 mmHg) - Contraindication to CPAP treatment |
Country | Name | City | State |
---|---|---|---|
Canada | Institut Universitaire de Cardiologie et de Pneumologie de Québec (IUCPQ) | Québec | |
France | Hopital Universitaire de Grenoble | La Tronche | |
France | Clinique Pasteur | Toulouse | |
Switzerland | Hopitaux Universitaires de Genève | Genève | |
Switzerland | Centre Hospitalier Universitaire Vaudois | Lausanne |
Lead Sponsor | Collaborator |
---|---|
AGIR à Dom | University Hospital, Grenoble |
Canada, France, Switzerland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Systolic arterial blood pressure assessed by 24-hours home blood pressure monitoring | Systolic arterial blood pressure assessed by 24-hours home blood pressure monitoring | To baseline at 12 weeks | |
Secondary | diastolic arterial blood pressure assessed by 24-hours home blood pressure monitoring | diastolic arterial blood pressure assessed by 24-hours home blood pressure monitoring | To baseline at 12 weeks | |
Secondary | Mean arterial blood pressure assessed by 24-hours home blood pressure monitoring | Mean arterial blood pressure assessed by 24-hours home blood pressure monitoring | To baseline at 12 weeks | |
Secondary | Change in physical activity: number of hour per day of physical activity | Change in physical activity: number of hour per day of physical activity | To baseline at 12 weeks | |
Secondary | pulse wave velocity | pulse wave velocity | To baseline at 12 weeks | |
Secondary | Change in physical activity : Metabolic Equivalents (METS) | Change in physical activity : Metabolic Equivalents (METS) | To baseline at 12 weeks | |
Secondary | Change in physical activity : Number of steps per day | Change in physical activity : Number of steps per day | To baseline at 12 weeks | |
Secondary | Change in sleep duration: Sleep to lying position duration ratio | Change in sleep duration: Sleep to lying position duration ratio | To baseline at 12 weeks |
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