The Effect of Eszopiclone on the Arousal Threshold in Sleep Apnea Syndrome
Primary Purpose
Obstructive Sleep Apnea
Status
Completed
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Eszopiclone
Placebo
Sponsored by
About this trial
This is an interventional basic science trial for Obstructive Sleep Apnea focused on measuring Obstructive sleep apnea, Arousal threshold, Sedative medication, upper airway
Eligibility Criteria
Inclusion Criteria:
- 18-64 years old
- Untreated obstructive sleep apnea
Exclusion Criteria:
- Nadir SaO2 <70% on a baseline PSG
- Medications known to affect either sleep, breathing or muscle activity
- Major co-morbidities apart from sleep apnea
- Allergy to lidocaine, oxymetazoline HCl, or eszopiclone
- Women who are pregnant
Sites / Locations
- Brigham and Women's Hospital, Division of Sleep Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Eszopiclone
Sugar Pill
Arm Description
Eszopiclone 3mg prior to sleep (1 night)
Sugar Pill (placebo) prior to sleep (1 night)
Outcomes
Primary Outcome Measures
Apnea Hypopnea Index
number of respiratory events per hour of sleep Respiratory events last for at least 10 seconds and are associated with a decrease in blood oxygenation or a cortical arosual from sleep. AHI values are typically categorized as 5-15/hr = mild; 15-30/hr = moderate; and > 30/h = severe
Secondary Outcome Measures
Arousal Threshold
quantified using an epiglottic pressure transducer in CmH2O
Nadir Overnight Oxygen Saturation
Nadir overnight oxygen saturation (%)
Sleep Duration
total sleep duration
Full Information
NCT ID
NCT01102270
First Posted
April 2, 2010
Last Updated
April 14, 2017
Sponsor
Brigham and Women's Hospital
Collaborators
Sumitomo Pharma America, Inc., National Heart, Lung, and Blood Institute (NHLBI)
1. Study Identification
Unique Protocol Identification Number
NCT01102270
Brief Title
The Effect of Eszopiclone on the Arousal Threshold in Sleep Apnea Syndrome
Official Title
A Double-Blind Randomized Physiological Study Examining the Effects of Eszopiclone on the Arousal Threshold and Obstructive Sleep Apnea Severity
Study Type
Interventional
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
January 2009 (undefined)
Primary Completion Date
August 2009 (Actual)
Study Completion Date
May 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
Collaborators
Sumitomo Pharma America, Inc., National Heart, Lung, and Blood Institute (NHLBI)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to find out whether taking eszopiclone (Lunesta) changes the breathing effort required to briefly wake people with obstructive sleep apnea from sleep (respiratory arousal threshold). We would like to see if taking eszopiclone can reduce the severity of obstructive sleep apnea in some people (those that have a low respiratory arousal threshold; i.e. wake up easily to respiratory stimuli).
Detailed Description
Obstructive sleep apnea is an exceedingly common disease with major neurocognitive and cardiovascular consequences. The current primary treatment e.g. Continuous positive airway pressure (CPAP) is effective but poorly tolerated by many patients particularly those with mild-moderate disease. Secondary treatments such as oral appliances to advance the mandible or surgical procedures to enlarge the airway are commonly appealing to the patient. However, these approaches have only modest success in reducing apnea frequency to an acceptable level. Thus, finding tolerable and effective therapy for sleep apnea remains an important objective.
The causes of sleep apnea vary between patients. Targeted therapy according to the underlying causes of sleep apnea in individual patients is likely to be most effective. However, current therapeutic options for sleep apnea are quite limited. The purpose of this physiological research study is to determine if taking eszopiclone (Lunesta)changes the breathing effort required to briefly wake people with obstructive sleep apnea from sleep (the arousal threshold) and if administration of the sedative medication eszopiclone (Lunesta) to certain sleep apnea patients (those with a low arousal threshold ie wake up easily) would be beneficial.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obstructive Sleep Apnea
Keywords
Obstructive sleep apnea, Arousal threshold, Sedative medication, upper airway
7. Study Design
Primary Purpose
Basic Science
Study Phase
Early Phase 1
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
17 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Eszopiclone
Arm Type
Active Comparator
Arm Description
Eszopiclone 3mg prior to sleep (1 night)
Arm Title
Sugar Pill
Arm Type
Placebo Comparator
Arm Description
Sugar Pill (placebo) prior to sleep (1 night)
Intervention Type
Drug
Intervention Name(s)
Eszopiclone
Other Intervention Name(s)
Lunesta
Intervention Description
3mg tablet once prior to sleep
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
sugar pill
Intervention Description
1 placebo capsule prior to sleep
Primary Outcome Measure Information:
Title
Apnea Hypopnea Index
Description
number of respiratory events per hour of sleep Respiratory events last for at least 10 seconds and are associated with a decrease in blood oxygenation or a cortical arosual from sleep. AHI values are typically categorized as 5-15/hr = mild; 15-30/hr = moderate; and > 30/h = severe
Time Frame
8 hour In-Laboratory Polysomnogram (PSG)
Secondary Outcome Measure Information:
Title
Arousal Threshold
Description
quantified using an epiglottic pressure transducer in CmH2O
Time Frame
8 hour In-Laboratory Polysomnogram (PSG)
Title
Nadir Overnight Oxygen Saturation
Description
Nadir overnight oxygen saturation (%)
Time Frame
8 hour In-Laboratory Polysomnogram (PSG)
Title
Sleep Duration
Description
total sleep duration
Time Frame
8 hour In-Laboratory Polysomnogram (PSG)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18-64 years old
Untreated obstructive sleep apnea
Exclusion Criteria:
Nadir SaO2 <70% on a baseline PSG
Medications known to affect either sleep, breathing or muscle activity
Major co-morbidities apart from sleep apnea
Allergy to lidocaine, oxymetazoline HCl, or eszopiclone
Women who are pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Atul Malhotra, MD
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brigham and Women's Hospital, Division of Sleep Medicine
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
published
Citations:
PubMed Identifier
21269278
Citation
Eckert DJ, Owens RL, Kehlmann GB, Wellman A, Rahangdale S, Yim-Yeh S, White DP, Malhotra A. Eszopiclone increases the respiratory arousal threshold and lowers the apnoea/hypopnoea index in obstructive sleep apnoea patients with a low arousal threshold. Clin Sci (Lond). 2011 Jun;120(12):505-14. doi: 10.1042/CS20100588.
Results Reference
result
Learn more about this trial
The Effect of Eszopiclone on the Arousal Threshold in Sleep Apnea Syndrome
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