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NCT05881512 · ClinicalTrials.gov registry record · NA
Early Feasibility Study of Transcutaneous Upper Airway Stimulation in Obstructive Sleep Apnea
A NA study of Obstructive Sleep Apnea and OSA, sponsored by Somnial.
- Completed
- Registry status
- NA
- Development phase
- 12
- Enrollment target
- 1
- Study location
NCT05881512 is a NA study of Obstructive Sleep Apnea and OSA that has completed, run by Somnial. The registered enrollment target is 12 participants, below the 222-participant average among 155 other Obstructive Sleep Apnea trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05881512, a NA study of Obstructive Sleep Apnea and OSA, has completed, sponsored by Somnial.
- COMPLETED
- Registry status
- NA
- Development phase
- 12 participants
- Enrollment target
- 1
- Study location
Study Summary
Early feasibility study to estimate the functionality of a novel intervention based on non-invasive transcutaneous electrical stimulation of the hypoglossal nerve to reduce the Apnea Hypopnea Index (AHI).
Conditions Studied
Interventions
- DEVICE Transcutaneous Upper Airway Stimulation Device
Study Locations (1)
New York
- United Diagnostics - Commack
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 12 participants |
| Start Date | 2022-09-12 |
| Est. Completion | 2023-02-22 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05881512
The ClinicalTrials.gov registry entry for NCT05881512 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 222-participant average among 155 other Obstructive Sleep Apnea trials with a reported enrollment target (95% lower). The listed sponsor is Somnial, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Obstructive Sleep Apnea appearing as the primary indexed condition, and to 1 intervention - of which Transcutaneous Upper Airway Stimulation Device is the first listed.
NCT05881512 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT05881512 about?
NCT05881512 is a clinical study titled "Early Feasibility Study of Transcutaneous Upper Airway Stimulation in Obstructive Sleep Apnea". Early feasibility study to estimate the functionality of a novel intervention based on non-invasive transcutaneous electrical stimulation of the hypoglossal nerve to reduce the Apnea Hypopnea Index (AHI).
What is the current status of trial NCT05881512?
This trial is currently completed. It is a NA study. The enrollment target is 12 participants. The study started on 2022-09-12. Estimated completion is 2023-02-22.
What conditions does trial NCT05881512 study?
This clinical trial studies the following conditions: Obstructive Sleep Apnea, OSA.
What interventions are being tested in trial NCT05881512?
The interventions under investigation include: Transcutaneous Upper Airway Stimulation Device (DEVICE).
Who is sponsoring clinical trial NCT05881512?
This trial is sponsored by Somnial, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05881512 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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