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Clinical Trials/NCT01896661
NCT01896661CompletedPhase 3

The Effect of Antihypertensive Agents Over Sleep Apnea: a Randomized Controlled Trial

Hospital de Clinicas de Porto Alegre1 site in 1 country53 target enrollmentStarted: December 2014Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 3
Status
Completed
Enrollment
53
Locations
1
Primary Endpoint
Apnea-Hypopnea Index

Study Overview

Brief Summary

Obstructive sleep apnea and hypertension are well-known cardiovascular risk factors. Their control could reduce the burden of heart disease across populations. There are several drugs to control hypertension, but the only consistently beneficial treatment to reduce apneas is continuous positive airway pressure. The demonstration that one drug could improve sleep apnea and hypertension would support a novel approach in the treatment of both diseases. The role of fluid retention in sleep apnea is known for several decades. The role of diuretics is well established in hypertension but was never appropriately tested in sleep apnea. Besides to test the efficacy of these drugs, this study will help to understand the mechanisms that link hypertension and sleep apnea and its treatment.

Detailed Description

This is a randomized, double-blind, clinical trial, comparing the association of Chlorthalidone plus amiloride 25 and 5 mg daily, versus amlodipine 10 mg daily as first drug option in patients older than 40 years of age with Stage I hypertension (140-159/90-99 mmHg) and moderate obstructive sleep apnea (15-30 apneas/hour of sleep). The primary outcomes will be the variation of apneas/hour and blood pressure. The secondary outcomes will be adverse events, somnolence scale (Epworth), ventilatory parameters and C reactive protein. The follow up will last 8 weeks. The sample size will be of 29 participants per group. The project was approved by the Ethics committee of our institution.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
40 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients older than 40 years of age
  • Stage I hypertension (140-159/90-99 mmHg) and moderate obstructive sleep apnea (10-40 apneas/hour of sleep)

Exclusion Criteria

  • Low life expectancy
  • Other indications for the use of diuretics or calcium channel blocker -Intolerance or contraindications to the study drugs
  • Pregnancy
  • Established cardiovascular disease (myocardial infarction
  • Heart failure)
  • Use of more than one drug for hypertension
  • Secondary hypertension
  • Participation in other clinical trial in previous 6 months

Arms & Interventions

Diuretics

Experimental

Chlorthalidone plus amiloride 25 and 5 mg daily, taking in the morning

Intervention: Diuretics (Drug)

Calcium Channel Blockers

Active Comparator

Amlodipine 10 mg daily, taking in the morning

Intervention: Calcium Channel Blockers (Drug)

Outcomes

Primary Outcomes

Apnea-Hypopnea Index

Time Frame: 8 weeks

Number of apneas/hour

Blood Pressure

Time Frame: 8 weeks

Secondary Outcomes

  • Adverse events(8 weeks)
  • Somnolence scale (Epworth) and ventilatory parameters(8 weeks)
  • C reactive protein(8 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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