Clinical trial Recruiting at 1 site Phase 4 Interventional Ages 60 to 89

Investigating treatments for sleep apnea in elderly veterans

Official title: Pathophysiology-Guided Therapy for Sleep Apnea in the Elderly

Run by VA Office of Research and Development · NCT02703220 · Data updated 2026-11-12

This study is testing whether oxygen, finasteride, and acetazolamide can help elderly veterans with sleep apnea breathe better while they sleep.

More Sleep Apnea trials

Quick facts

PhasePhase 4
Study typeInterventional
Ages60 Years to 89 Years
SexAll
Enrollment100 (estimated)
SponsorVA Office of Research and Development
Federal
Locations1 site (Detroit, Michigan)
StatusRecruiting
StartedJuly 3, 2015
Main results expectedJuly 30, 2027
Study endsDecember 31, 2027
Registry record updatedAugust 21, 2026
Trial IDNCT02703220 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are elderly adults aged 60 and older with mild to moderate sleep apnea.

Probably not a fit

Patients with severe sleep apnea or significant comorbid conditions such as cardiac disease or severe pulmonary disorders may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to explore the effectiveness of oxygen, finasteride, and acetazolamide in reducing sleep apnea among elderly veterans. It focuses on understanding how these interventions can modulate breathing stability during sleep by affecting ventilatory control mechanisms. The research will compare cerebrovascular reactivity between younger and older adults to identify key factors contributing to sleep apnea in the elderly. Ultimately, the goal is to develop novel therapies that improve the quality of life for elderly veterans suffering from sleep-disordered breathing.

Why it matters

Potential benefit: If successful, this study could lead to new treatment options for elderly patients with sleep apnea, improving their overall health and quality of life.

How similar studies have gone: While alternative therapies for sleep apnea have been explored, this specific approach targeting elderly veterans is novel and has not been extensively tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adults with mild to moderate sleep apnea with Apnea-Hypopnea Index (AHI)\>/=5 to 20/hour with central, obstructive, mixed apneas and hypopneas
* For the finasteride protocol elderly men with above criteria will be enrolled

Exclusion Criteria:

* Patients with severe sleep apnea (Apnea-Hypopnea Index (AHI)\>20/hour)
* Patients with history of prostate cancer
* Males with hypogonadism
* History of cardiac disease, including myocardial infarction
* Bypass surgery
* Atrial and ventricular tachy-bradycardias
* Systolic congestive heart failure and Cheyne-Stokes respiration
* Current unstable angina
* Stroke
* Schizophrenia
* Untreated hypothyroidism
* Seizure disorder
* Preexisting renal failure and liver disorders
* Failure to give informed consent.
* Patients with significant pulmonary diseases by history and abnormal pulmonary function testing, including moderate obstructive/restrictive lung/chest wall disorders with resting oxygen saturation of \<96% or on supplemental oxygen
* Patients on certain medications including:

  * study drugs
  * sympathomimetics/parasympathomimetics or their respective blockers
  * narcotics
  * antidepressants
  * anti-psychotic agents
  * other central nervous system (CNS) altering medications
  * current alcohol, tobacco or recreational drug use
* Patients with Body mass index (BMI)\>34 kilograms per square meter (kg/m2) will be excluded to avoid the effects of morbid obesity on pulmonary mechanics and ventilatory control
* Elderly with unstable gait or mobility issues that may preclude safe participation
* Individuals with allergy to finasteride or acetazolamide will be excluded from the specific protocol
* Pregnant women

Where it's running

  • John D. Dingell VA Medical Center, Detroit, MI
    Detroit, Michigan, United States
    Recruiting

Study contacts

  • Principal investigator: Susmita Chowdhuri, MD MS — John D. Dingell VA Medical Center, Detroit, MI
  • Study coordinator: Ruchi Rastogi, MS
  • Email: ruchi.rastogi@va.gov
  • Phone: (313) 576-4464

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.