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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02428478
Other study ID # BWH-2014P001033A
Secondary ID
Status Completed
Phase Phase 2
First received April 21, 2015
Last updated July 14, 2016
Start date March 2015
Est. completion date March 2016

Study information

Verified date July 2016
Source Brigham and Women's Hospital
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Obstructive sleep apnea (OSA) is common and has major health implications but treatment options are limited. OSA patients show a marked reduction in upper airway (UA) dilator muscle activity at sleep onset and this phenomenon leads to increased collapsibility of UA compared to normal subjects. Until recently, the search for medicines to activate pharyngeal muscles in sleeping humans has been discouraging. However, exciting new animal research has shown that drugs with noradrenergic and antimuscarinic effects can restore pharyngeal muscle activity to waking levels. In this protocol the investigators will test the effect of desipramine (a tricyclic antidepressant with strong noradrenergic and antimuscarinic effects) on genioglossus muscle activity (EMG GG) during sleep in healthy control subjects.


Description:

Two overnight sleep studies, a placebo night and a drug night, will be performed approximately one week apart in random order. The placebo or drug will be administered 2 hours before lights out. At least 15 minutes of quiet wakefulness will be recorded to quantify the subject's awake EMG GG activity. Subjects will then sleep in the lateral position to minimize pharyngeal resistance similar to previous studies of this kind.

The same will be done for stable NREM and REM sleep (free of arousals and other artifacts). Both NREM and REM sleep will be analyzed, recognizing that REM is less frequent on these drugs.

During the second part of the night, the subjects will be connected to a modified continuous positive airway pressure (CPAP) machine (Pcrit3000, Respironics) which can provide a wide range of pressures between 20 and -20 cmH2O in order to modify upper airway pressure and measure change in EMG GG as a function of epiglottic pressure (muscle responsiveness).


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date March 2016
Est. primary completion date November 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Healthy control subjects

Exclusion Criteria:

- Cardiovascular disease other than well controlled hypertension

- Depression

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Desipramine
200 mg administered 2 hour before normal sleep time
Placebo


Locations

Country Name City State
United States Sleep Disorders Research Program Brigham and Women's Hospital Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Brigham and Women's Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Effect of desipramine on electromyography of genioglossus muscle activity during sleep in control healthy subjects. EMG GG Sleep values will be expressed as %wakefulness value and compared between nights. Activity of GG EMG will be measured during wakefulness and sleep stages as % of maximum activation obtained pushing the tongue against closed teeth during wakefulness (GG%max). Sleep values will then be expressed as %wakefulness value and compared between nights. 1 night No
Secondary Effect of desipramine of genioglossus muscle responsiveness to increased pharyngeal resistance during sleep in healthy controls. Data will be expressed as change in GG EMG for cmH2O change in epiglottic pressure. (GG%max/cmH2O). Epiglottic pressure will be altered using a modified CPAP machine (Pcrit3000, Respironics) which can provide a range of pressure between 20 and -20 cmH2O 1 night No
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