Phase 4
N=20
The Impact of Venlafaxine on Apnea Hypopnea Index in Obstructive Sleep Apnea
Obstructive Sleep Apnea
Bottom Line
View on ClinicalTrials.gov: NCT02714400 ↗Enrolled (actual)
20
Serious AEs
0.0%
Results posted
Apr 2020
Primary outcome: Primary: The Apnea Hypopnea Index — 40.5; 46.1 Events per Hour of Sleep
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 4
- Interventions
- Venlafaxine (Drug); Placebo (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of California, San Diego
- Primary completion
- Jul 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY The Apnea Hypopnea Index |
40.5; 46.1 | — |
| PRIMARY Nadir Oxygen Level During Sleep |
82.0; 81.5 | — |
| SECONDARY Loop Gain |
0.58; 0.56 | — |
| SECONDARY Arousal Threshold |
115.6; 118.6 | — |
| SECONDARY Sleep Efficiency |
63.1; 72.5 | — |
Summary
The investigators hypothesis is that obstructive sleep apnea (OSA) patients with a low arousal threshold may wake up too early during a respiratory event, before upper airway muscles can be activated to achieve stable ventilation. Thus, strategies to manipulate the respiratory arousal threshold could potentially improve the quality of sleep and sleep disordered breathing. Agents that raise arousal threshold are therefore likely to benefit some patients with OSA. The overall goal of this project is to determine the importance of the arousal threshold in OSA, determine which patients might benefit from a raised arousal threshold, and test this hypothesis by using pharmacological manipulation of the arousal threshold to achieve this goal.
Eligibility Criteria
Inclusion Criteria
- Ages 18-70 years
- sleep study (with apnea hypopnea index>5)
- Diagnosis of obstructive sleep apnea
Exclusion Criteria
- Any known cardiac (apart from treated hypertension), pulmonary (including uncontrolled asthma), renal, neurologic (including epilepsy), neuromuscular, or hepatic disease.
- Susceptible to stomach ulcers.
- co-administration of MAO inhibitors intended to treat psychiatric disorders (concurrently or within 14 days of discontinuing the MAO inhibitor); initiation of MAO inhibitor intended to treat psychiatric disorders within 7 days of discontinuing venlafaxine; initiation in patients receiving linezolid or intravenous methylene blue
- Pregnant women.
- History of hypersensitivity to Afrin, Lidocaine (all Aims) or venlafaxine
- History of bleeding diathesis and/or gastrointestinal bleeding.
- Glaucoma and Urinary Retention
- Use of any medications that may affect sleep or breathing.
- Use of any medications that have known interaction with venlafaxine and the interaction may significantly increase the risk of the subject or decrease the therapeutic effect of the medication.
- A psychiatric disorder, other than mild depression; e.g. schizophrenia, bipolar disorder, major depression, panic or anxiety disorders.
- Substantial cigarette (>5/day), alcohol (>3oz/day) or use of illicit drugs.
- More than 10 cups of beverages with caffeine (coffee, tea, soda/pop) per day.
- Desaturations to below 70% lasting greater than 10 seconds in duration per event
Data sourced from ClinicalTrials.gov (NCT02714400). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.