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Improving 24-hour Blood Pressure in Obstructive Sleep Apnea

Primary Purpose

Obstructive Sleep Apnea

Status
Withdrawn
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
Continuous Positive Airway Pressure CPAP
Telmisartan 80mg
Alpha-Lipoic Acid 600mg
Microcrystalline Cellulose
Sponsored by
University of British Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obstructive Sleep Apnea focused on measuring Telmisartan, Alpha-Lipoic Acid, Continuous Positive Airway Pressure, 24-hour blood pressure

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Apnea/Hypopnea Index (AHI) greater than/equal to 15 events per hour of sleep
  • No prior use of CPAP
  • Body mass index less than 30kg/m2
  • Does not take ARBs or angiotensin converting enzyme inhibitors for blood pressure control
  • Females of childbearing potential on an effective or highly effective means of contraception

Exclusion Criteria:

  • Prescribed and/or taking the following medications: diuretics (including potassium-sparing diuretics), Digoxin, lithium salts, and/or nonsteroidal anti-inflammatory drugs
  • Over the counter supplements that affect the cardiovascular system, such as fish oils, vitamins, or other antioxidants
  • History of heart failure
  • History of myocardial infarction
  • History of coronary artery disease
  • History of stroke
  • History of diabetes mellitus
  • History of impaired renal function
  • History of chronic obstructive pulmonary disease
  • History of asthma
  • History of central sleep apnea
  • Smoked within the past year
  • Hypotensive (Systolic blood pressure (SBP) <90 mmHg and diastolic blood pressure (DBP) <60 mmHg)
  • Females who do not have a means of contraception, are pregnant, planning to become pregnant, and/or are breast-feeding

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    Combined Treatment

    Placebo Control

    Arm Description

    Subjects will be given 80 mg/day Telmisartan + 600 mg/day Alpha-Lipoic Acid. Subjects will also be prescribed CPAP therapy by their physician. Subjects will be instructed to use their CPAP device according to their physician's guidelines.

    Subjects will be given placebo capsules. Subjects will also be prescribed CPAP therapy by their physician. Subjects will be instructed to use their CPAP device according to their physician's guidelines.

    Outcomes

    Primary Outcome Measures

    Change in 24-hour blood pressure
    Systolic, diastolic, and mean arterial blood pressure (mmHg)

    Secondary Outcome Measures

    Full Information

    First Posted
    July 10, 2019
    Last Updated
    May 17, 2023
    Sponsor
    University of British Columbia
    Collaborators
    Heart and Stroke Foundation of Canada, Michael Smith Foundation for Health Research
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04021550
    Brief Title
    Improving 24-hour Blood Pressure in Obstructive Sleep Apnea
    Official Title
    Combined Treatment of Angiotensin Receptor Blocker and Antioxidant Supplementation as a Novel Adjunctive Therapy for 24-hour Blood Pressure Improvement in Obstructive Sleep Apnea
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2023
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Covid-19 Pandemic prevented this study from beginning
    Study Start Date
    May 2023 (Anticipated)
    Primary Completion Date
    December 2026 (Anticipated)
    Study Completion Date
    December 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of British Columbia
    Collaborators
    Heart and Stroke Foundation of Canada, Michael Smith Foundation for Health Research

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This study examines the combined effects of an angiotensin receptor blocker (ARB), antioxidant supplementation, and continuous positive airway pressure (CPAP) therapy on the lowering of 24-hour blood pressure in persons with moderate to severe Obstructive Sleep Apnea (OSA). All participants will undergo CPAP therapy as prescribed by their doctor; however, half of the participants will receive the combined ARB and antioxidant treatment while the other half of the participants will receive a placebo.
    Detailed Description
    OSA is a sleep disorder characterized by repetitive collapses (apneas) or partial collapses (hypopneas) of the upper airway. These airway obstructions result in intermittent reductions in arterial oxygen saturation (hypoxia), which causes a reflexive increase in sympathetic activation and systemic vasoconstriction. Resumption of breathing results in transient surges in blood pressure (BP) that can reach as high as 240/130 mm/Hg. OSA effects up to 24% of the adult population and evidence suggests a causal relationship between OSA and cardiovascular disease (CVD) development. While the exact mechanisms are unknown, data from animal and human models suggest that exposure to chronic intermittent hypoxia (IH) plays a significant role in the pathogenesis of cardiovascular comorbidity. Persons with OSA exhibit increased daytime sympathetic activity, markers of oxidative stress, and vasoactive hormones, particularly angiotensin II, that contribute to systemic vasoconstriction. These factors contribute to early endothelial dysfunction and contribute to sustained elevations in BP. While CPAP is the gold standard OSA treatment, adherence rates are low and evidence suggests that treatment does not reduce the rates of CVD in large population-based studies. Telmisartan is a receptor blocker for angiotensin II and not only has BP lowering effects, but also has unique anti-inflammatory properties and beneficial influences on endothelial function. The addition of an antioxidant supplement may increase the reactive oxygen species scavenging capacity and, in combination with ARB treatment, may provide more robust effects on BP in persons with OSA.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Obstructive Sleep Apnea
    Keywords
    Telmisartan, Alpha-Lipoic Acid, Continuous Positive Airway Pressure, 24-hour blood pressure

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Early Phase 1
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Combined Treatment
    Arm Type
    Experimental
    Arm Description
    Subjects will be given 80 mg/day Telmisartan + 600 mg/day Alpha-Lipoic Acid. Subjects will also be prescribed CPAP therapy by their physician. Subjects will be instructed to use their CPAP device according to their physician's guidelines.
    Arm Title
    Placebo Control
    Arm Type
    Placebo Comparator
    Arm Description
    Subjects will be given placebo capsules. Subjects will also be prescribed CPAP therapy by their physician. Subjects will be instructed to use their CPAP device according to their physician's guidelines.
    Intervention Type
    Device
    Intervention Name(s)
    Continuous Positive Airway Pressure CPAP
    Intervention Description
    All subjects will be advised to use their continuous positive airway pressure (CPAP) in accordance to their physician's guidelines.
    Intervention Type
    Drug
    Intervention Name(s)
    Telmisartan 80mg
    Intervention Description
    Subjects in this group will receive 80mg/day of Telmisartan (an angiotensin receptor blocker). Treatments will be administered in pre-packaged blister packages. Subjects will take Telmisartan once per day for 6 weeks.
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Alpha-Lipoic Acid 600mg
    Intervention Description
    Subjects in this group will receive 600mg/day of Alpha-Lipoic Acid (an antioxidant). Treatments will be administered in pre-packaged blister packages. Subjects will take Alpha-Lipoic Acid once per day for 6 weeks.
    Intervention Type
    Other
    Intervention Name(s)
    Microcrystalline Cellulose
    Intervention Description
    Subjects in this group will receive two capsules of Microcrystalline Cellulose (placebo). Treatments will be administered in pre-packaged blister packages. Subjects will take placebo pills once per day for 6 weeks.
    Primary Outcome Measure Information:
    Title
    Change in 24-hour blood pressure
    Description
    Systolic, diastolic, and mean arterial blood pressure (mmHg)
    Time Frame
    Change from baseline of 24-hour systolic, diastolic, and mean arterial blood pressure at 6 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Apnea/Hypopnea Index (AHI) greater than/equal to 15 events per hour of sleep No prior use of CPAP Body mass index less than 30kg/m2 Does not take ARBs or angiotensin converting enzyme inhibitors for blood pressure control Females of childbearing potential on an effective or highly effective means of contraception Exclusion Criteria: Prescribed and/or taking the following medications: diuretics (including potassium-sparing diuretics), Digoxin, lithium salts, and/or nonsteroidal anti-inflammatory drugs Over the counter supplements that affect the cardiovascular system, such as fish oils, vitamins, or other antioxidants History of heart failure History of myocardial infarction History of coronary artery disease History of stroke History of diabetes mellitus History of impaired renal function History of chronic obstructive pulmonary disease History of asthma History of central sleep apnea Smoked within the past year Hypotensive (Systolic blood pressure (SBP) <90 mmHg and diastolic blood pressure (DBP) <60 mmHg) Females who do not have a means of contraception, are pregnant, planning to become pregnant, and/or are breast-feeding

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    21504246
    Citation
    Frampton JE. Telmisartan: a review of its use in cardiovascular disease prevention. Drugs. 2011 Apr 16;71(6):651-77. doi: 10.2165/11206710-000000000-00000.
    Results Reference
    background
    PubMed Identifier
    29036393
    Citation
    Khayat RN, Varadharaj S, Porter K, Sow A, Jarjoura D, Gavrilin MA, Zweier JL. Angiotensin Receptor Expression and Vascular Endothelial Dysfunction in Obstructive Sleep Apnea. Am J Hypertens. 2018 Feb 9;31(3):355-361. doi: 10.1093/ajh/hpx174.
    Results Reference
    background
    PubMed Identifier
    18807180
    Citation
    Khayat R, Patt B, Hayes D Jr. Obstructive sleep apnea: the new cardiovascular disease. Part I: Obstructive sleep apnea and the pathogenesis of vascular disease. Heart Fail Rev. 2009 Sep;14(3):143-53. doi: 10.1007/s10741-008-9112-z. Epub 2008 Sep 20.
    Results Reference
    background
    PubMed Identifier
    27542595
    Citation
    Rotenberg BW, Murariu D, Pang KP. Trends in CPAP adherence over twenty years of data collection: a flattened curve. J Otolaryngol Head Neck Surg. 2016 Aug 19;45(1):43. doi: 10.1186/s40463-016-0156-0.
    Results Reference
    background
    PubMed Identifier
    20522795
    Citation
    Pepin JL, Tamisier R, Barone-Rochette G, Launois SH, Levy P, Baguet JP. Comparison of continuous positive airway pressure and valsartan in hypertensive patients with sleep apnea. Am J Respir Crit Care Med. 2010 Oct 1;182(7):954-60. doi: 10.1164/rccm.200912-1803OC. Epub 2010 Jun 3.
    Results Reference
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