Sleep Apnea
Conditions
Brief summary
Currently, there is no pharmacological intervention for OSA that targets multiple pathophysiological deficits in combination. Here the investigators study the effect on sleep apnea severity of combinations of pharmacological agents that stimulate the pharyngeal muscles, stabilize ventilatory control, and increase the arousal threshold.
Detailed description
The primary goal of the current study is to determine the effect of combination therapy targeting phenotypic traits on OSA severity. Specifically, the investigators will assess the effect of combination pharmacological therapy on OSA severity as measured by the apnea-hypopnea index and the arousal index (co-primary outcome variables). The investigators will also estimate the effects of the interventions on the physiological traits responsible for OSA using polysomnography, namely: * Pharyngeal anatomy and its propensity towards collapse * The ability of the upper airway dilator muscles to activate and reopen the airway during sleep (i.e. neuromuscular compensation) * Arousal threshold from sleep (i.e. the propensity for hypopneas/apneas to lead to arousal and fragmented sleep). * Stability of the ventilatory control system feedback loop (i.e. loop gain). Baseline traits will be used to examine whether patient characteristics influence the responses to each combination of interventions (i.e. muscles, muscles plus loop gain, muscles plus arousal threshold).
Interventions
DRUGSAS0421a
treatment will be given for 3 days
DRUGSAS0421b
treatment will be given for 3 days
DRUGSAS0421c
treatment will be given for 3 days
DRUGplacebo
placebo will be given for 3 days
Sponsors
Apnimed
Brigham and Women's Hospital
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 79 Years
Healthy volunteers
No
Inclusion criteria
* Ages 18 - 79 years * Suspected or diagnosed OSA
Exclusion criteria
* Any uncontrolled medical condition * Current use of the medications under investigation * Use of medications expected to stimulate or depress respiration (including opioids, barbiturates, doxapram, almitrine, theophylline, 4-hydroxybutanoic acid). * Current use of hypnotic medications (trazodone, eszopiclone, benzodiazepines). * Current use of SNRIs/SSRIs or anticholinergic medications. * Conditions likely to affect obstructive sleep apnea physiology: neuromuscular disease or other major neurological disorder, heart failure (also below), or any other unstable major medical condition. * Respiratory disorders other than sleep disordered breathing: chronic hypoventilation/hypoxemia (awake SaO2 \< 92% by oximetry) due to chronic obstructive pulmonary disease or other respiratory conditions. * Other sleep disorders: periodic limb movements (periodic limb movement arousal index \> 10/hr), narcolepsy, or parasomnias. * Contraindications for SAS0421a and SAS0421b, including: * hypersensitivity to SAS0421a and SAS0421b (angioedema or urticaria) * pheochromocytoma * use of monoamine oxidase inhibitors * benign prostatic hypertrophy, urinary retention * untreated narrow angle glaucoma * bipolar disorder, mania, psychosis * history of major depressive disorder (age\<24). * history of attempted suicide or suicidal ideation within one year prior to screening * clinically significant constipation, gastric retention * pre-existing seizure disorders * clinically-significant kidney disorders (eGFR\<60 ml/min/1.73m2) * clinically-significant liver disorders * clinically-significant cardiovascular conditions * severe hypertension (SBP\>180 mmHg or DBP\>110 mmHg measured at baseline) * cardiomyopathy (LVEF\<50%) or heart failure * advanced atherosclerosis * history of cerebrovascular events * history of cardiac arrhythmias e.g., atrial fibrillation, QT prolongation * other serious cardiac conditions that would raise the consequences of an increase in blood pressure or heart rate * myasthenia gravis * pregnancy/breast-feeding * Additional contraindications for SAS0421c, including: * Use more than 500 mg/day of Aspirin * Allergies to this drug class * Adrenocortical insufficiency * Low sodium or potassium * hyperchloremic acidosis * Claustrophobia * Pregnancy or nursing
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Apnea-hypopnea index [AHI] | 3 days | Apneas and hypopneas per hour (3% desat and/or arousal), % change from baseline |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Hypoxic Burden | 3 days | Desaturation area under curve × event frequency |
| Arousal Index | 3 days | Number of arousals per hour (\>=3-sec), % change from baseline |
| Visual Analog Scale for Sleep Quality | 3 days | Sleep Quality 0-10 scale, 0 worst sleep quality, 10 best sleep quality |
| Visual Analog Scale for Waking Unrefreshed | 3 days | Waking Unrefreshed 0-10 scale, 0 extremely refreshed, 10 extremely unrefreshed |
Other
| Measure | Time frame | Description |
|---|---|---|
| Visual Analog Scale for Low Energy | 3 days | Low Energy 0-10 scale, 0 no trouble with energy, 10 extremely low energy |
| Visual Analog Scale for Treatment Satisfaction | 3 days | Treatment Satisfaction 0-10 scale, 0 extremely dissatisfied, 10 extremely satisfied |
| Proportion of Total Sleep Time in non-REM Stage 1 | 3 days | % Total sleep time |
| Visual Analog Scale for Excessive Fatigue | 3 days | Excessive Fatigue 0-10 scale, 0 no fatigue, 10 highly fatigued |
Countries
Australia, United States
Outcome results
None listed