Cardiovascular Phenotype Study in Patients With Obstructive Sleep Apnea Syndrome (SAS-HTA)
Recruitment status was Recruiting
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Purpose
Patients with obstructive sleep apnea syndrome have permanent variations of their hemodynamic parameters during the night : heart rate, arterial blood pressure, cardiac output. This is due to the repetition of respiratory events (obstructive apnea and hypopnea) leading to frequent micro-arousals. These disorders have several consequences : hypertension, NO-dependent vasodilatation impairment, baroreceptor reflex impairment, insulin resistance and other cardiovascular impairments.
| Condition | Intervention | Phase |
|---|---|---|
|
Obstructive Sleep Apnea Syndrome Hypertension |
Device: Positive airway pressure treatment Other: No positive airway pressure treatment |
Phase 0 |
| Study Type: | Interventional |
| Study Design: | Intervention Model: Factorial Assignment Masking: Open Label Primary Purpose: Health Services Research |
| Official Title: | Cardiovascular Phenotype Study in Patients With Obstructive Sleep Apnea Syndrome : Role of Hypertension |
- cardiovascular phenotype study in patients with non treated obstructive sleep apnea syndrome [ Time Frame: 6 years ] [ Designated as safety issue: No ]
- characterization of arterial blood pressure, sympathetic activity, functional and morphological cardiovascular modifications. Effect of a treatment of obstructive sleep apnea syndrome on those different parameters. [ Time Frame: 6 years ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 300 |
| Study Start Date: | March 2001 |
| Estimated Study Completion Date: | December 2008 |
| Estimated Primary Completion Date: | December 2003 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: SAS+HTA+
Obstructive sleep apnea syndrome and hypertension
|
Device: Positive airway pressure treatment
Positive airway pressure treatment as long as necessary
Other Name: CPAP treatment
|
|
Experimental: SAS+HTA-
non hypertensive patients with obstructive sleep apnea syndrome
|
Device: Positive airway pressure treatment
Positive airway pressure treatment as long as necessary
Other Name: CPAP treatment
|
|
Experimental: SAS-HTA+
hypertensive patients without obstructive sleep apnea syndrome
|
Other: No positive airway pressure treatment
No treatment
Other Name: No CPAP treatment
|
|
Experimental: SAS-HTA-
non hypertensive patients without obstructive sleep apnea syndrome
|
Other: No positive airway pressure treatment
No treatment
Other Name: No CPAP treatment
|
Detailed Description:
Objective of the study is to characterize the cardiovascular phenotype of patients with obstructive sleep apnea syndrome, relative to the presence of hypertension or not. Hypertension should not have been previously treated. 2 groups of apneic patients (SAS+HTA+ and SAS+HTA-) will be compared together, referred to group of non apneic but hypertensive patients (SAS-HTA+) and non apneic / non hypertensive patients (SAS-HTA-).
Apneic and hypertensive patients may have a sympathetic nervous system activation and a much more important vascular and baroreceptor reflex impairment, than non apneic but hypertensive patients.
During the study, a second visit as control will be done for apneic patients only, 3 to 6 months after SAS treatment setting.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- patients with or without obstructive sleep apnea syndrome (AHI > 15)
- patients with or without hypertension
Exclusion Criteria:
- known or expected secondary hypertension
- pathologies with consequences on arterial blood pressure regulation: Parkinson's disease, patients with renal or cardiac graft, severe heart failure
- drugs with consequences on arterial blood pressure regulation : vasoconstrictors, vasodilatators, béta-agonists, antagonists, nitrites, theophylline, dipyridamol, sildenafil, immunosuppressors, IMAO, neuroleptics, tricyclic antidepressants, corticoids or long-term oral (>10 days) non steroidal anti-inflammatory drugs, oestroprogestative treatments
- atrial fibrillation, frequent extrasystoles (> or = to 10/minute)
- bedridden patients
- night shift workers
- surgical or carotid stenting history
- subjects unwilling or unable to provide written, signed and dated informed consent
- patient previously treated for obstructive sleep apnea syndrome (positive airway pressure, forward mandible prosthesis, maxillofacial surgery
Contacts and Locations| Contact: Jean-Philippe JB BAGUET, PhD | 00330476764226 ext 64226 | JBaguet@chu-grenoble.fr |
| Contact: Jean-Louis JP PEPIN, PhD | 00330476768473 ext 68473 | JPepin@chu-grenoble.fr |
| France | |
| Cardiology and hypertension service | Recruiting |
| Grenoble, Isère, France, 38000 | |
| Contact: Jean-Philippe JB BAGUET, PhD 0033476764226 ext 64226 JBaguet@chu-grenoble.fr | |
| Contact: Jean-Louis JP PEPIN, PhD 0033476768473 ext 68473 JPepin@chu-grenoble.fr | |
| Principal Investigator: | Jean-Philippe JB BAGUET, PhD | University Hospital, Grenoble |
More Information
Publications:
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | BAGUET Jean-Philippe, PhD, University Hospital Grenoble |
| ClinicalTrials.gov Identifier: | NCT00764218 History of Changes |
| Other Study ID Numbers: | DGS2001/0398 |
| Study First Received: | September 30, 2008 |
| Last Updated: | September 30, 2008 |
| Health Authority: | France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis) |
Keywords provided by University Hospital, Grenoble:
|
Obstructive sleep apnea syndrome Hypertension Cardiovascular phenotype |
Additional relevant MeSH terms:
|
Apnea Hypertension Sleep Apnea Syndromes Sleep Apnea, Obstructive Respiration Disorders Respiratory Tract Diseases Signs and Symptoms, Respiratory |
Signs and Symptoms Vascular Diseases Cardiovascular Diseases Sleep Disorders, Intrinsic Dyssomnias Sleep Disorders Nervous System Diseases |
ClinicalTrials.gov processed this record on May 16, 2013