Clinical trial

Rescuing OSA Patients Unable to Tolerate CPAP Using Endotype-Targeted Combination Drug Therapy: a Randomized, Double-Blind, Placebo-Controlled Trial

Name
191990
Description
Obstructive sleep apnea (OSA) is common and associated with many adverse health consequences, but many patients are unable to tolerate standard therapies such as continuous positive airway pressure (CPAP) and thus remain untreated. Single-drug therapies have shown promising results in treating sleep apnea, but on average patients have only experienced partial relief. Multi-drug therapy may offer a more effective treatment approach. The goal of this study is to test the effect of combination therapy with three FDA-approved drugs (Diamox \[acetazolamide\], Lunesta \[eszopiclone\] +/- Effexor \[venlafaxine\]) on OSA severity and physiology.
Trial arms
Trial start
2020-12-01
Estimated PCD
2022-01-27
Trial end
2022-01-27
Status
Completed
Phase
Early phase I
Treatment
Acetazolamide
Acetazolamide tablet (encapsulated)
Arms:
Dual-Therapy, then Placebo, then Single/Triple-Therapy, Placebo, then Dual-Therapy, then Single/Triple-Therapy
Other names:
Diamox
Eszopiclone
Eszopiclone tablet (encapsulated)
Arms:
Dual-Therapy, then Placebo, then Single/Triple-Therapy, Placebo, then Dual-Therapy, then Single/Triple-Therapy
Other names:
Lunesta
Placebo
Sugar capsule manufactured to match encapsulated Acetazolamide/Eszopiclone
Arms:
Dual-Therapy, then Placebo, then Single/Triple-Therapy, Placebo, then Dual-Therapy, then Single/Triple-Therapy
Venlafaxine
Venlafaxine capsule
Arms:
Dual-Therapy, then Placebo, then Single/Triple-Therapy, Placebo, then Dual-Therapy, then Single/Triple-Therapy
Other names:
Effexor
Size
20
Primary endpoint
Apnea Hypopnea Index (AHI)
3 nights
Eligibility criteria
Inclusion Criteria: * BMI 18-40 kg/m2 * Untreated Moderate or Severe OSA (AHI during supine NREM sleep \>15/h) with a fraction of hypopneas \>25% of all events Exclusion Criteria: * Pregnancy * Breastfeeding * Prisoners * Adherent with effective therapy for OSA * Other known untreated sleep fragmenting disorder, such as periodic limb movement disorder, or narcolepsy * Inability to sleep supine for overnight sleep studies * Circadian rhythm disorder * Unrevascularized coronary artery disease, angina, prior heart attack or stroke, congestive heart failure * Uncontrolled hypertension (systolic blood pressure \>160mmHg, diastolic blood pressure \>95mmHg) * Presence of tracheostomy * Hospitalization within the past 90 days * Prior peptic ulcer disease, esophageal varices, or gastrointestinal bleeding (\< 5 years) * Prior gastric bypass surgery * Chronic liver disease or end-stage kidney disease * Active illicit substance use or \>2 oz daily alcohol use (i.e. \>2 12 oz bottles of beers, \>2 5 oz glasses of wine, \>2 1.5 oz glasses of hard liquor such as spirits, gin, whiskey, etc.) * Psychiatric disease, other than well controlled depression/anxiety * Cognitive impairment, inability to provide consent, or inability to complete research procedures (e.g. questionnaires that are only available/validated in English) * Chronically using study drugs or drugs with similar pharmacodynamic effects (acetazolamide - carbonic anhydrase inhibitors, eszopiclone - benzodiazepine receptor agonists, venlafaxine - serotonin/norepinephrine reuptake inhibitors and other antidepressants) * Regular use of medications known to affect control of breathing (opioids, benzodiazepines, theophylline) * Contraindications to taking study drugs, including allergies to any of the drugs or sulfa allergy; concomitant use of antidepressants, opioids, sedatives/hypnotics, thiazide diuretics or angiotensin-receptor blockers; or severe nocturnal hypoxia (SpO2 nadir \<70% on diagnostic sleep study).
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'CROSSOVER', 'interventionModelDescription': 'Randomized, double-blind, placebo-controlled, cross-over trial.', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 20, 'type': 'ACTUAL'}}
Updated at
2024-05-29

1 organization

3 products

1 drug

2 indications