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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02385864
Other study ID # 2013-A00908-37
Secondary ID
Status Recruiting
Phase N/A
First received February 26, 2015
Last updated March 4, 2016
Start date September 2015
Est. completion date February 2017

Study information

Verified date March 2016
Source University Hospital, Grenoble
Contact Gilles Barone-Rochette, MD, PhD
Phone (+33) 4 76 76 51 72
Email gbarone@chu-grenoble.fr
Is FDA regulated No
Health authority France: Comité consultatif sur le traitement de l'information en matière de recherche dans le domaine de la santéFrance: Commission nationale de l'informatique et des libertés
Study type Observational

Clinical Trial Summary

Resistant hypertension is defined as uncontrolled blood pressure (BP ≥ 140/90mmHg) despite the current use of three or more antihypertensive drugs at full doses, including a diuretic. Obstructive Sleep Apnea (OSA) is at high risk for cardiovascular morbidity and is highly prevalent in patients with resistant hypertension.

The prospective observational POP-ART study will assess the efficacy of continuous positive airway pressure (CPAP) treatment on BP in patients with resistant hypertension and collect data from usual care.


Description:

Obstructive Sleep Apnea is highly prevalent in patients with resistant hypertension and several studies have assessed the effect of CPAP treatment on BP.

But only few studies have raised data about the effect of CPAP treatment on BP in patients with resistant hypertension.

Hypertension is moreover associated with increased arterial stiffness, but no data are available in patients with resistant hypertension.

The purpose of this study is to demonstrate that OSA has a major impact in resistant hypertension, whose effects on BP and arterial stiffness can partially be reversible with CPAP treatment.


Recruitment information / eligibility

Status Recruiting
Enrollment 166
Est. completion date February 2017
Est. primary completion date August 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Patient with resistant hypertension uncontrolled by 3 or more antihypertensive agents

- Patient with severe OSA (apnea-hypopnea index > 30 or > or equal to 15 with excessive daytime sleepiness), or with mild to moderate OSA without excessive daytime sleepiness, or without OSA.

- Ambulatory patient

Exclusion Criteria:

- Body mass index =40 kg/m2

- Other identifiable causes of hypertension

- Contraindication to CPAP treatment or patient already treated with CPAP

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
France Bordeaux University Hospital Bordeaux
France Clinique du Tondu Bordeaux
France Clinique des Eaux Claires, Groupe Hospitalier Mutualiste Grenoble
France Grenoble University Hospital Grenoble

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Grenoble

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mean variation in BP at 6 months, assessed by 24h ambulatory BP monitoring 6 months from baseline assessment No
Secondary OSA prevalence in patients with resistant hypertension 6 months No
Secondary BP variability assessed by home self BP measurments 6 months No
Secondary Arterial stiffness assessed by pulse wave velocity and QKD interval 6 months No
Secondary Antihypertensive treatment consumption 6 months No
Secondary CPAP treatment observance 6 months No
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