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Cycloserine in the Treatment of Sleep Apnea

Primary Purpose

Sleep Apnea Syndromes

Status
Terminated
Phase
Phase 1
Locations
Canada
Study Type
Interventional
Intervention
Cycloserine
Placebo
Sponsored by
University of Manitoba
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sleep Apnea Syndromes focused on measuring Sleep apnea, Hypoglossal Nerve, N-methyl-D-aspartate receptors, Cycloserine, Short-term potentiation

Eligibility Criteria

21 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Moderate to severe obstructive or central sleep apnea (Apnea Hypopnea Index > 30/hr).
  • Minimum Oxygen saturation during respiratory events >70% throughout sleep during the clinical sleep study.

Exclusion Criteria:

  • Contraindication to the use of cycloserine, namely history of allergy to cycloserine, seizures, depression, severe anxiety or psychosis, excessive use of alcohol or renal failure.
  • Past or current history of tuberculosis
  • Hypercapnia > 55 millimeters of mercury during the diagnostic clinical sleep study.
  • Neuromuscular disease.
  • Obesity-hypoventilation syndrome.
  • Pregnancy.
  • Significant co-morbidities: Dialysis-dependant renal failure, severe asthma or chronic lung disease, congestive heart failure, previous stroke.
  • Recent (within 3 months) myocardial infarction or Active coronary ischemia event.

Sites / Locations

  • University of Calgary
  • Sleep Disorders Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Cycloserine

Placebo

Arm Description

Cycloserine, 250 mg capsules by mouth, one hour prior to initiation of sleep study, single dose

Placebo, sugar capsule by mouth, one hour prior to initiation of sleep study, single dose

Outcomes

Primary Outcome Measures

Change in Apnea-hypopnea index (AHI)
Baseline apnea-hypopnea index in first night and upon end of the second sleep study, performed one week apart

Secondary Outcome Measures

Improvement in total sleep time
Improvement in average oxygen saturation

Full Information

First Posted
November 18, 2015
Last Updated
September 12, 2019
Sponsor
University of Manitoba
Collaborators
University of Calgary
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1. Study Identification

Unique Protocol Identification Number
NCT02735694
Brief Title
Cycloserine in the Treatment of Sleep Apnea
Official Title
Cycloserine in the Treatment of Sleep Apnea
Study Type
Interventional

2. Study Status

Record Verification Date
November 2015
Overall Recruitment Status
Terminated
Why Stopped
Analysis of initial sample shows negative results.
Study Start Date
September 2015 (Actual)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
November 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Manitoba
Collaborators
University of Calgary

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study is being conducted to determine whether cycloserine is effective for the treatment of sleep apnea. Cycloserine is an antibiotic that has been extensively used in the treatment tuberculosis. However, more recently it was shown to enhance memory responses. Cycloserine may enhance the response of respiratory muscles to apnea and potentially reduce the severity of sleep disordered breathing.
Detailed Description
The passive human upper airway (UA) is a collapsible tube with a relatively high compliance. At atmospheric luminal pressure, its cross-sectional area varies considerably. Subjects in whom the pharynx is closed, or nearly closed, at near atmospheric pressure require an upper airway dilating force to maintain adequate ventilation. During wakefulness pharyngeal dilator muscles (dilators) provide the necessary force to permit an adequate flow, regardless of how collapsible the pharynx is. This dilator activity is substantially lost at sleep onset. Subjects in whom the passive UA cannot permit adequate ventilation must recruit dilators through reflex mechanisms if they are to remain asleep. Recent studies have shown that activation of the muscles that open the airway in the course of obstructive apneas persists to a variable degree after the relief of obstruction, evidencing the presence of memory for prior activation in the the brain centers that supply the dilator muscles. Short-term potentiation (STP) is a neuro-physiological mechanism that results in a time-dependent increase in motor activity, that is not explainable by changes in stimulus intensity, and which persists after disappearance of the stimulus ( "after-discharge"). STP is well documented in diaphragmatic responses to chemical stimuli. Prominent STP in upper airway muscles would promote a stronger dilator response to upper airway occlusion. The after-discharge would also help to maintain dilator activity following the ventilatory phase of obstructive events, thereby mitigating recurrence of obstruction. Patients with obstructive sleep apnea (OSA) vary greatly in the extent to which this memory or STP is present. The investigators postulate that interventions that could potentiate the development of memory for prior activation would mitigate the recurrence of apneas and reduce the severity of obstructive sleep apnea. The same interventions, those that enhance memory for prior activation, would also likely improve central apneas in that these apneas represent loss of diaphragm activity following hyperventilation. Memory for prior activation of the diaphragm has been well documented in the past and appears to be defective in such patients. There has been extensive research into methods of improving neural memory. Cycloserine, an antibiotic that has been, and continues to be, used extensively in the treatment of drug-resistant tuberculosis, was shown to be effective in promoting memory in small doses (much less than those used for tuberculosis) both in animals and humans. We, therefore, propose that cycloserine has the potential of enhancing the memory properties of neurones supplying pharyngeal muscles and propose to study the effect of using it on the severity of sleep apneas of the obstructive and central varieties. Patients who have been diagnosed with OSA following routine clinical sleep studies will be asked to participate. Participation involves agreeing to two additional full night studies in the sleep laboratory, separated by 1 week. Both studies will be identical to the routine clinical studies, except that the patient will be asked to swallow a capsule containing either placebo or 250 mg cycloserine 1 to 2 hours prior to going to sleep. The order of the Placebo and Test nights will be randomized. The patient will be monitored continuously by a dedicated, senior polysomnography technologist.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Apnea Syndromes
Keywords
Sleep apnea, Hypoglossal Nerve, N-methyl-D-aspartate receptors, Cycloserine, Short-term potentiation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
18 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cycloserine
Arm Type
Active Comparator
Arm Description
Cycloserine, 250 mg capsules by mouth, one hour prior to initiation of sleep study, single dose
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo, sugar capsule by mouth, one hour prior to initiation of sleep study, single dose
Intervention Type
Drug
Intervention Name(s)
Cycloserine
Other Intervention Name(s)
Seromycin
Intervention Description
Capsule containing 250 mg of Cycloserine
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Sugar capsule
Intervention Description
Sugar capsule manufactured to mimic Cycloserine 250 mg capsule
Primary Outcome Measure Information:
Title
Change in Apnea-hypopnea index (AHI)
Description
Baseline apnea-hypopnea index in first night and upon end of the second sleep study, performed one week apart
Time Frame
Baseline and one week
Secondary Outcome Measure Information:
Title
Improvement in total sleep time
Time Frame
Baseline and one week
Title
Improvement in average oxygen saturation
Time Frame
One week
Other Pre-specified Outcome Measures:
Title
Improvement in the awakening and arousals index
Description
number of awakenings and arousals per hour of sleep as measurement of sleep continuity.
Time Frame
One week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Moderate to severe obstructive or central sleep apnea (Apnea Hypopnea Index > 30/hr). Minimum Oxygen saturation during respiratory events >70% throughout sleep during the clinical sleep study. Exclusion Criteria: Contraindication to the use of cycloserine, namely history of allergy to cycloserine, seizures, depression, severe anxiety or psychosis, excessive use of alcohol or renal failure. Past or current history of tuberculosis Hypercapnia > 55 millimeters of mercury during the diagnostic clinical sleep study. Neuromuscular disease. Obesity-hypoventilation syndrome. Pregnancy. Significant co-morbidities: Dialysis-dependant renal failure, severe asthma or chronic lung disease, congestive heart failure, previous stroke. Recent (within 3 months) myocardial infarction or Active coronary ischemia event.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Magdy K Younes, Md, PhD
Organizational Affiliation
University of Manitoba
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Calgary
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2N 4N1
Country
Canada
Facility Name
Sleep Disorders Centre
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R3C 1A2
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
No plan has been made on sharing individual data

Learn more about this trial

Cycloserine in the Treatment of Sleep Apnea

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