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Sleep and Breathing in the General Population - Chemical Stimuli

Primary Purpose

Sleep-disordered Breathing

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Zolpidem
No Treatment
Sponsored by
Wayne State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sleep-disordered Breathing focused on measuring Sleep-disordered Breathing, central sleep apnea

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Men and women Veterans with central sleep apnea, defined as Apnea Hypopnea Index (AHI)>15/hour with CAHI>5/hour, will be included in the experiments.

Exclusion Criteria:

  • less than 18 years old
  • pregnant or breastfeeding female
  • have severe respiratory disease that require to be on oxygen
  • recent health event that may affect the ability to participate in the study,
  • Body Mass Index (BMI) is >40 kg/m2
  • significant insomnia
  • mental instability
  • recent health event that may affect sleep
  • if at any time the principal investigator (PI) identifies that a certain drug is not suitable, or are unable to use the device that is used to treat sleep apnea, will be not be allowed to participate in the study

Sites / Locations

  • John D. Dingell VA Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Zolpidem, then No Treatment

No Treatment, then Zolpidem

Arm Description

Participants will be administered zolpidem for the first night study, and No Treatment during the second night study.

Participants will be administered zolpidem for the second night study, and No Treatment during the first night study.

Outcomes

Primary Outcome Measures

The Central Apnea-hypopnea Index
The number of central apneas and hypopneas per hour of sleep was obtained from polysomnography studies.
Respiratory Arousal Index
A measure of the frequency of respiratory-related arousals during sleep

Secondary Outcome Measures

CO2 Reserve
CO2 reserve is the requisite change to induce central apnea is referred to as the CO2 reserve, which can be positive or negative. CO2 reserve is defined as the difference between the eupneic end-tidal CO2 pressure and the end-tidal CO2 pressure induced by the ventilation protocol that is sufficient to trigger a central apnea as defined by the American Academy of Sleep Medicine.
Controller Gain
Controller gain is a ventilatory response to changes in end-tidal PCO2. Controller gain was calculated by dividing the difference in minute ventilation between the post-mechanical ventilation induced by the ventilation protocol and steady-state respiration by the difference in the end-tidal CO2 pressure between the mechanical ventilation and steady-state respiration.
Stead-State Plant Gain (mmHg
Plant gain is a blood gas response to a change in ventilation. This measure represents the effectiveness of the "plant" in eliminating CO2. Steady-state plant gain was calculated from the ratio of end-tidal CO2 to minute ventilation during stable respiration.
Respiratory Arousal Threshold
The nadir pressure in the upper airway (supra-glottic pressure) prior to the occurrence of an arousal

Full Information

First Posted
January 20, 2021
Last Updated
April 2, 2022
Sponsor
Wayne State University
Collaborators
National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT04720547
Brief Title
Sleep and Breathing in the General Population - Chemical Stimuli
Official Title
Sleep and Breathing in Health and Disease (Part 2A - Chemical Stimuli, Sleep and Breathing in the General Population)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
July 3, 2018 (Actual)
Primary Completion Date
February 29, 2020 (Actual)
Study Completion Date
February 29, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Wayne State University
Collaborators
National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Central sleep apnea (CSA) is a common condition and its treatment remains elusive. The focus of this proposal is to identify the role of the physiologic path involving cortical arousals in CSA by decreasing arousal frequency using the pharmacological agent zolpidem. The goal is to identify the acute effects of administering zolpidem on sleep and respiratory outcomes, and subsequently, its effect on the severity of CSA and propensity to develop CSA. This study will shed light on the mechanisms underlying CSA that involve cortical arousals and will guide future therapeutic interventions for CSA.
Detailed Description
The literature suggests that zolpidem may be effective in the treatment of central sleep apnea (CSA). However, evidence regarding the efficacy of zolpidem and the underlying mechanisms involved in its effect on CSA are not well-studied. Furthermore, respiratory-related arousals are hypothesized to contribute CSA symptoms and severity. The aim of the study is to determine the effect of decreasing respiratory-related arousals on the propensity to develop central apnea. The investigators hypothesize that administration of the nonbenzodiazepine hypnotic zolpidem will decrease the frequency of respiratory-related arousals, lower the central apnea-hypopnea index, and widen the CO2 reserve during sleep in patients with CSA compared to no treatment. Participants will complete a night study on a low dose of zolpidem and another night study without zolpidem in a crossover manner. The order of night studies is randomized. The results will help unveil the role of arousals in CSA and the acute effect of zolpidem on CSA severity and the propensity to CSA.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep-disordered Breathing
Keywords
Sleep-disordered Breathing, central sleep apnea

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Model Description
After an initial assessment to determine eligibility, participant complete two in-lab night studies in a randomized manner including one night with the administration of zolpidem and another without zolpidem.
Masking
Outcomes Assessor
Masking Description
Personnel conducting assessment of outcomes and data analysis are blinded to treatment.
Allocation
Randomized
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Zolpidem, then No Treatment
Arm Type
Experimental
Arm Description
Participants will be administered zolpidem for the first night study, and No Treatment during the second night study.
Arm Title
No Treatment, then Zolpidem
Arm Type
Experimental
Arm Description
Participants will be administered zolpidem for the second night study, and No Treatment during the first night study.
Intervention Type
Drug
Intervention Name(s)
Zolpidem
Other Intervention Name(s)
Ambien
Intervention Description
A nonbenzodiazepine hypnotic
Intervention Type
Other
Intervention Name(s)
No Treatment
Intervention Description
The Control condition in which participants do not receive medication.
Primary Outcome Measure Information:
Title
The Central Apnea-hypopnea Index
Description
The number of central apneas and hypopneas per hour of sleep was obtained from polysomnography studies.
Time Frame
one night
Title
Respiratory Arousal Index
Description
A measure of the frequency of respiratory-related arousals during sleep
Time Frame
one night
Secondary Outcome Measure Information:
Title
CO2 Reserve
Description
CO2 reserve is the requisite change to induce central apnea is referred to as the CO2 reserve, which can be positive or negative. CO2 reserve is defined as the difference between the eupneic end-tidal CO2 pressure and the end-tidal CO2 pressure induced by the ventilation protocol that is sufficient to trigger a central apnea as defined by the American Academy of Sleep Medicine.
Time Frame
one night
Title
Controller Gain
Description
Controller gain is a ventilatory response to changes in end-tidal PCO2. Controller gain was calculated by dividing the difference in minute ventilation between the post-mechanical ventilation induced by the ventilation protocol and steady-state respiration by the difference in the end-tidal CO2 pressure between the mechanical ventilation and steady-state respiration.
Time Frame
one night
Title
Stead-State Plant Gain (mmHg
Description
Plant gain is a blood gas response to a change in ventilation. This measure represents the effectiveness of the "plant" in eliminating CO2. Steady-state plant gain was calculated from the ratio of end-tidal CO2 to minute ventilation during stable respiration.
Time Frame
one night
Title
Respiratory Arousal Threshold
Description
The nadir pressure in the upper airway (supra-glottic pressure) prior to the occurrence of an arousal
Time Frame
one night

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Men and women Veterans with central sleep apnea, defined as Apnea Hypopnea Index (AHI)>15/hour with CAHI>5/hour, will be included in the experiments. Exclusion Criteria: less than 18 years old pregnant or breastfeeding female have severe respiratory disease that require to be on oxygen recent health event that may affect the ability to participate in the study, Body Mass Index (BMI) is >40 kg/m2 significant insomnia mental instability recent health event that may affect sleep if at any time the principal investigator (PI) identifies that a certain drug is not suitable, or are unable to use the device that is used to treat sleep apnea, will be not be allowed to participate in the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
M Safwan Badr, MD, MBA
Organizational Affiliation
John D. Dingell VA Medical Center, Detroit, MI
Official's Role
Principal Investigator
Facility Information:
Facility Name
John D. Dingell VA Medical Center
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35286569
Citation
Ahmad B, Sankari A, Eshraghi M, Aldwaikat A, Yarandi H, Zeineddine S, Salloum A, Badr MS. Effect of Zolpidem on nocturnal arousals and susceptibility to central sleep apnea. Sleep Breath. 2023 Mar;27(1):173-180. doi: 10.1007/s11325-022-02593-3. Epub 2022 Mar 14.
Results Reference
derived

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Sleep and Breathing in the General Population - Chemical Stimuli

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