Pilot Study of a Self-Supporting Nasopharyngeal Airway in Hypotonia (ssNPA)
Primary Purpose
Sleep Apnea, Obstructive, Hypotonia, Child, Only
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
ssNPA
Sponsored by
About this trial
This is an interventional treatment trial for Sleep Apnea, Obstructive focused on measuring Obstructive sleep apnea, Hypotonia, Nasal airway, Tolerability
Eligibility Criteria
Inclusion Criteria:
- hypotonia
- obstructive sleep apnea on polysomnogram with AHI>=10
- presence of at least one symptom of OSA (such as snoring 3 or more nights per week, daytime sleepiness, or hyperactive/inattentive behaviors)
Exclusion Criteria:
- AHI <10
- any reason why ssNPA may not be suitable
- Psychiatric, medical, or social factors likely to invalidate assessments, make adherence with ssNPA highly unlikely or make local follow-up at 8 weeks unfeasible
- Safe Continuous positive airway pressure therapy (CPAP) use is possible and tolerated
- Supraglottic airway collapse
- Distal airway stenosis
- Tracheobronchomalacia
- Active COVID 19 infection
- Need for anticoagulative therapy
- Bleeding disorder
- More than mild elevation of end tidal carbon dioxide (ETCO2) or transcutaneous carbon dioxide (TCO2) values >60 mmHg for >10% of sleep time
- Restrictive thoracic disorders
- Silicone, lidocaine, neosynephrine allergy
Sites / Locations
- C.S. Mott Children's Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
ssNPA
Arm Description
self-supporting nasopharyngeal airway to be used nightly for approximately 8 weeks.
Outcomes
Primary Outcome Measures
Ability to tolerate
Score of >=7 on Likert scale 0-10 in at least 60% of participants (higher score is better)
Comfort
Score of >=6 on Likert scale 0-10 in at least 60% of participants (higher score is better)
Ease of use
Score of >=5 on Likert scale 0-10 in at least 60% of participants (higher score is better)
Secondary Outcome Measures
Snoring
Less frequent snoring
Daytime sleepiness
Reduction in Epworth Sleepiness Scale score (0-24; lower score is better)
Sleep quality
Higher score in parent report of sleep quality on scale 0-10 (higher score is better)
Device design
Device optimization and manufacturing in a clean/sterile manner in 100% of cases
Insertion protocol
Optimize insertion protocol with ease of insertion >= 5 on Likert scale of 1-10 in 60% of participants (higher score is better)
Full Information
NCT ID
NCT04846400
First Posted
April 13, 2021
Last Updated
November 10, 2022
Sponsor
University of Michigan
Collaborators
National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI)
1. Study Identification
Unique Protocol Identification Number
NCT04846400
Brief Title
Pilot Study of a Self-Supporting Nasopharyngeal Airway in Hypotonia
Acronym
ssNPA
Official Title
Pilot Study of Novel Nasopharyngeal Airway Device for Treating Upper Airway Obstruction in Pediatric Hypotonia
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
May 6, 2022 (Actual)
Primary Completion Date
June 27, 2022 (Actual)
Study Completion Date
June 27, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan
Collaborators
National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Children with hypotonic upper airway obstruction have a high prevalence of severe obstructive sleep apnea, which if not treated has significant clinical consequence. Available treatment approaches, such as surgery and positive airway pressure, show limited efficacy and adherence. The multidisciplinary team has developed and now proposes to further test a non-surgical, well-tolerated nasopharyngeal airway device that in initial patients has resolved even extremely severe obstructive sleep apnea, and improved patient and family quality of life.
Detailed Description
There is a critical need for safe and effective treatment options for persistent obstructive sleep apnea (OSA) in patients with Hypotonic Upper Airway Obstruction (HUAO). HUAO encompass conditions such as cerebral palsy, hypoxic encephalopathy, syndromic tone anomalies, and neuromuscular disorders, and typically share a similar pattern of multisite upper airway collapse. OSA is characterized by recurrent episodes of partial or complete upper airway obstruction during sleep with associated arousals and/ or oxygen desaturations. Of hypotonic patients with symptoms of sleep disordered breathing, one quarter have moderate OSA, and more than half have severe OSA. Thus, not only are patients more likely to have OSA, but it is likely to be much more severe. Currently available treatment options, ranging from palliative care to tracheostomy, often fail to fully meet the needs of these patients. The multidisciplinary team has developed a dramatically effective non-surgical nasopharyngeal airway stent that has demonstrated good tolerability in hypotonic patients. This initial phase will test an enhanced version of the device for acceptability and tolerability. Critically, insertion, adherence, and compliance protocols will be optimized for preparation of the full trial.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Apnea, Obstructive, Hypotonia, Child, Only
Keywords
Obstructive sleep apnea, Hypotonia, Nasal airway, Tolerability
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
2 (Actual)
8. Arms, Groups, and Interventions
Arm Title
ssNPA
Arm Type
Experimental
Arm Description
self-supporting nasopharyngeal airway to be used nightly for approximately 8 weeks.
Intervention Type
Device
Intervention Name(s)
ssNPA
Intervention Description
The ssNPA is a self-supporting nasopharyngeal airway, a stent that is a non-surgical alternative to treat severe OSA
Primary Outcome Measure Information:
Title
Ability to tolerate
Description
Score of >=7 on Likert scale 0-10 in at least 60% of participants (higher score is better)
Time Frame
8 weeks
Title
Comfort
Description
Score of >=6 on Likert scale 0-10 in at least 60% of participants (higher score is better)
Time Frame
8 weeks
Title
Ease of use
Description
Score of >=5 on Likert scale 0-10 in at least 60% of participants (higher score is better)
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Snoring
Description
Less frequent snoring
Time Frame
8 weeks
Title
Daytime sleepiness
Description
Reduction in Epworth Sleepiness Scale score (0-24; lower score is better)
Time Frame
8 weeks
Title
Sleep quality
Description
Higher score in parent report of sleep quality on scale 0-10 (higher score is better)
Time Frame
8 weeks
Title
Device design
Description
Device optimization and manufacturing in a clean/sterile manner in 100% of cases
Time Frame
8 weeks
Title
Insertion protocol
Description
Optimize insertion protocol with ease of insertion >= 5 on Likert scale of 1-10 in 60% of participants (higher score is better)
Time Frame
8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
hypotonia
obstructive sleep apnea on polysomnogram with AHI>=10
presence of at least one symptom of OSA (such as snoring 3 or more nights per week, daytime sleepiness, or hyperactive/inattentive behaviors)
Exclusion Criteria:
AHI <10
any reason why ssNPA may not be suitable
Psychiatric, medical, or social factors likely to invalidate assessments, make adherence with ssNPA highly unlikely or make local follow-up at 8 weeks unfeasible
Safe Continuous positive airway pressure therapy (CPAP) use is possible and tolerated
Supraglottic airway collapse
Distal airway stenosis
Tracheobronchomalacia
Active COVID 19 infection
Need for anticoagulative therapy
Bleeding disorder
More than mild elevation of end tidal carbon dioxide (ETCO2) or transcutaneous carbon dioxide (TCO2) values >60 mmHg for >10% of sleep time
Restrictive thoracic disorders
Silicone, lidocaine, neosynephrine allergy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David A Zopf, MD
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
C.S. Mott Children's Hospital
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
For this initial pilot of 5 participants there are no plans to share data.
Learn more about this trial
Pilot Study of a Self-Supporting Nasopharyngeal Airway in Hypotonia
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