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Central and Peripheral Blood Pressure in Treatment of Obstructive Sleep Apnea.

Central and Peripheral 24-h Blood Pressure Monitoring in Patients With Hypertension and Obstructive Sleep Apnea Before and After Treatment With Continuous Positive Airway Pressure.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02078778
Acronym
HOSI
Enrollment
20
Registered
2014-03-05
Start date
2014-02-28
Completion date
2017-03-31
Last updated
2015-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension, Obstructive Sleep Apnea

Keywords

Continuous airway pressure, Hypertension, Obstructive sleep apnea

Brief summary

The purpose of this study is to examine the effect on blood pressure of 3 months of treatment with continuous positive airway pressure (CPAP) in patients with obstructive sleep apnea (OSA). Hypothesis: 1. Central 24-h blood pressure (BP) monitoring hedges day fluctuations in blood pressure more accurately than peripheral 24-h BP monitoring, because the measurement is painless and does not interfere with the patient / subject's activities during the daytime or nighttime sleep. 2. Blood pressure is elevated in patients with OSA and falls during treatment with CPAP. 3\. The renal treatment of salt and water is abnormal in OSA, improved during treatment with CPAP. 4\. Quality of life improves during treatment with CPAP

Detailed description

Approximately 20 patients with hypertension and moderate to severe OSA are treated with CPAP 3 months to examine the treatment effect on blood pressure throughout the day, but especially nocturnal, renal treatment of salt and water, and quality of life. Before and after 3 months of CPAP treatment is made central and peripheral 24-h ambulatory blood pressure monitoring, 24-h urine collection and blood samples.

Interventions

DEVICECPAP

3 months of CPAP treatment

Sponsors

Erling Bjerregaard Pedersen
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
55 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* chronic kidney disease (CKD stage I and II), eGFR 60-90 ml/min/1.73 m2 or eGFR\> 90 ml/min/1.73 m2 and proteinuria or other signs of kidney damage. * Obstructive sleep apnea, apnea hypopnea index (AHI) \> 15 (moderate to severe) * Both men and women * 55-70 years * Signed consent form

Exclusion criteria

* Lack of desire to participate * Malignant disease * Abuse of drugs or alcohol * Pregnant and breastfeeding * Incompensated heart failure * Atrial fibrillation * Liver disease (Alanine aminotransferase (ALT) \> 200) * Severe chronic obstructive pulmonary disease (Forced expiratory volume in 1 second \<50% predicted) * Blood pressure difference between the right and left arm\> 10/10 mmHg

Design outcomes

Primary

MeasureTime frameDescription
difference in systolic peripheral BP at night3 monthsThe difference in systolic BP at night by peripheral BP days before and after 3 months of treatment of OSA with CPAP in patients with hypertension.

Secondary

MeasureTime frameDescription
Difference i BP throughout the day3 monthsThe difference in systolic BP and diastolic BP throughout the day, in the daytime and in nighttime between measurements with peripheral and central 24-h blood pressure monitoring before and after 3 months of treatment with CPAP.
Correlation between degree of OSA and kidney function on effect of treatment3 monthsThe correlation between the treatment effect on blood pressure levels on the one hand and the severity of OSA prior to initiation of treatment and renal function as measured by estimated glomerular filtration rate (eGFR) on the other.
Difference i central systolic BP3 monthsThe difference in systolic BP at night in central BP days before and after 3 months of treatment of OSA with CPAP in patients with hypertension.
Plasma renin concentration (PRC), plasma angiotensin II (p-AngII), plasma aldosterone (p-Aldo), plasma vasopressin (P-AVP) and plasma endothelin (p-endothelin).3 monthsChanges in PRC, p-AngII, p-Aldo. P-AVP and p-endothelin in blood samples before and after 3 month of treatment.
Quality of life3 monthsChanges in the quality of life before and after treatment of OSA with CPAP.
urine auquaporine2 (u-AQP2) and urine epithelial Natrium channel (u-ENaC)3 monthsChanges in U-AQP2 and u-ENaC in 24-h urine samples before and after 3 month of treatment.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026