Effect of Continuous Positive Airway Pressure (CPAP) Treatment in the Control of Refractory Hypertension
The working hypothesis for the present study is that treatment with CPAP in patients with an sleep apnea (IAH>15) and AHT-r is capable of producing significant reductions in blood-pressure levels.
This hypothesis is supported by four proven findings:
- -sleep apnea is an independent risk factor for arterial hypertension (1).
- -The greater the number of RSD, the greater the loss of control over blood-pressure levels (1).
- -The prevalence of sleep apnea in patients with AHT refractory to treatment is very high (11,12).
- -Treatment of patients with sleep apnea and AHT-r with CPAP succeeds in significantly reducing blood-pressure levels in the only (small-scale) studies undertaken to date (14,15).
To evaluate the effect of treatment with CPAP on blood-pressure levels in patients with AHT refractory to medical treatment.
- To evaluate the effect of treatment with CPAP on the various elements assessed in BP (systolic/diastolic; daytime/nighttime, etc) and the circadian profile (dipper/non-dipper/raiser patterns; variability and homogeneity of blood-pressure levels, etc) obtained during a 24-hour out-patient study (AMPA).
- To analyze the related variables or subgroups of patients most affected by treatment with CPAP.
- To evaluate the effect of CPAP on the levels of some of the biological variables involved in the pathogenesis of AHT-r (renin, angiotensin, aldosterone, atrial natriuretic factor, etc).
|Study Design:||Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Investigator, Outcomes Assessor)
Primary Purpose: Treatment
|Official Title:||Effect of CPAP Treatment in the Control of Refractory Hypertension|
- Effect on blood pressure levels [ Time Frame: Before and six months after CPAP treatment ] [ Designated as safety issue: Yes ]
- Effect on night blood pressure pattern [ Time Frame: Befor and six month after CPAP treatment ] [ Designated as safety issue: Yes ]
|Study Start Date:||June 2008|
|Study Completion Date:||February 2012|
|Primary Completion Date:||December 2011 (Final data collection date for primary outcome measure)|
No Intervention: B
Group B. Only Usual Control
Group A: Cpap treatment plus Usual control
Pressure device on airway to maintain it open
Other Name: Continuous positive airway pressure
OBJECTIVE. To evaluate the effect of continuous positive airway pressure (CPAP) treatment on the blood-pressure (BP) levels of patients with refractory arterial hypertension (AHT-r).
METHODS: Multicenter randomized study with parallel groups and blind final evaluation.
Patients will be recruited from AHT, nephrology or internal medicine outpatient clinics and will satisfy the criteria for AHT-r (patients requiring 3 anti-AHT drugs at recommended doses to maintain their blood-pressure levels within AMPA [24-hours ambulatory monitoring of blood pressure values) excluding those forms of secondary AHT and those patients with incapacitating hypersomnia that need immediate treatment. In all, 210 patients will be included (105 per arm for intention to treat analysis) in accordance with the calculation of the sample size needed including drop-outs to evaluate a clinically significant minimum drop of 4-5 mmHg in the mean BP and the number of centers (21 centers; 10 patients per center). They will all be subjected to a complete clinical history, an AMPA study, a blood test (with serum retained for a later determination of biological mediators) and a sleep study. Those patients with an AHI>15 will be randomized to receive CPAP vs habitual control. The treatment will last 3 months. The same variables that were measured before the randomization will be analyzed again for the purposes of comparison. The comparison of results will be undertaken on the basis of an intention-to-treat and per-protocol analyses based on adherence to CPAP treatment at different cutoff of hours /day by means of an ANOVA two-way analysis (one of them being time).
Please refer to this study by its ClinicalTrials.gov identifier: NCT00616265
|General Hospital of Requena|
|Valencia, Spain, 42340|
|Principal Investigator:||Miguel Angel Martínez-Garcia, MD||Sociedad Española de Neumología y Cirugía Torácica|