Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT05846490

Impact of Obstructive Sleep Apnea (OSA) Treatment on Blood Pressure Control in Chronic Kidney Disease

Led by University of Sao Paulo · Updated on 2024-06-11

150

Participants Needed

1

Research Sites

120 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The role of obstructive sleep apnea (OSA) on chronic kidney disease (CKD) is not clear. This randomized clinical trial will test the impact of OSA treatment on blood pressure (BP) and on the estimated glomerular filtration rate (eGFR) in patients with CKD IIIb and IV (eGFR 44-15 ml/min). A polygraph will be performed to assess the presence of OSA (defined by an apnea-hypopnea index ≥15 events/hour). Patients with OSA will be randomized to use continuous positive upper airway pressure (CPAP) or to maintain optimized clinical treatment for BP control. Antihypertensive medication adjustments will be allowed using a standard protocol for both groups by the same researcher, who will not have access to CPAP follow-up. In addition to clinical (including BP and ambulatory BP monitoring, ABPM) and laboratory assessments at baseline, we will follow up at 3 months, 6 months, 9 months and 12 months after randomization of the proposed outcomes. Target organ damage analyses, such as the retina and echocardiography, will be performed at baseline and after 1 year of randomization. Primary objective: to compare the effect of CPAP on the need to adjust antihypertensive medication to control systolic BP (\<130mmHg) in patients with CKD; secondary objectives: 1) to evaluate the reduction in systolic and diastolic BP by office and ABPM; 2) assessment of nocturnal BP dipping; 3) to evaluate the impact of OSA treatment with CPAP on eGFR during follow-up; 4) to evaluate the impact of OSA treatment with CPAP on the evolution of albuminuria; 5) assessment of other target organ damage such as retinopathy and cardiac remodeling; 6) to evaluate the impact of OSA treatment with CPAP on the possible delay for renal replacement therapy or end-stage renal disease (eGFR \<15ml/min and dialysis); 7) to evaluate the impact of OSA treatment with CPAP on the quality of life of patients with CKD. With a significance level of 5% and study power of 90%, two-tailed hypothesis testing, 74 patients with OSA per group, i.e., 148 patients in total, will be required to assess the primary endpoint (we estimate that 25% and 50% of patients in control and CPAP groups will not need to adjust their antihypertensive medication at follow-up, respectively).

CONDITIONS

Official Title

Impact of Obstructive Sleep Apnea (OSA) Treatment on Blood Pressure Control in Chronic Kidney Disease

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed diagnosis of hypertension defined by use of oral antihypertensive drugs or systolic BP greater than 140 mmHg and/or diastolic BP greater than 90 mmHg on 2 office measurements or greater than 130/80 mmHg by 24-hour ambulatory blood pressure monitoring (ABPM).
  • Estimated glomerular filtration rate (eGFR) between 45 ml/min/1.73m2 and 15 ml/min/1.73m2 using the CKD-EPI equation, and patient is in conservative treatment for chronic kidney disease.
Not Eligible

You will not qualify if you...

  • Professional drivers.
  • Users of home supplemental oxygen.
  • Patients currently receiving treatment for obstructive sleep apnea.
  • Pregnant women.
  • Patients with malignant tumors or terminal illnesses.
  • Patients with severe asthma or chronic obstructive pulmonary disease.
  • Patients diagnosed with systemic lupus erythematosus, amyloidosis, or systemic sclerosis.
  • Patients with a history of solid organ transplants.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Fernanda Trani Ferreira

São Paulo, Brazil

Actively Recruiting

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Research Team

L

Luciano Drager, MD, PhD

CONTACT

F

Fernanda Trani Ferreira, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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