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NCT06698809 · ClinicalTrials.gov registry record · NA
Obstructive Sleep Apnea Therapeutic Intervention for REsiDual Sleepiness
A NA study of Obstructive Sleep Apnea and Sleepiness, sponsored by NYU Langone Health.
- Recruiting
- Registry status
- NA
- Development phase
- 22
- Enrollment target
- 1
- Study location
NCT06698809 is a NA study of Obstructive Sleep Apnea and Sleepiness that is actively recruiting participants, run by NYU Langone Health. The registered enrollment target is 22 participants, below the 221-participant average among 155 other Obstructive Sleep Apnea trials with a reported enrollment target (90% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06698809, a NA study of Obstructive Sleep Apnea and Sleepiness, is actively recruiting participants, sponsored by NYU Langone Health.
- RECRUITING
- Registry status
- NA
- Development phase
- 22 participants
- Enrollment target
- 1
- Study location
Study Summary
Obstructive sleep apnea (OSA) is a sleep disorder that is commonly treated using positive airway pressure, yet 50% of patients still experience residual sleepiness after successful therapy. A potential neuromodulation strategy that can decrease residual sleepiness is transcranial photobiomodulation (tPBM). tPBM is a neuromodulatory treatment that uses red and/or near infrared light to penetrate the cortex and can alter both cerebral metabolism and blood flow. However, this potential has never been explored before directly in sleep disordered individuals. This project aims to explore the effect of tPBM on sleepiness and understand the potential neural mechanism of tPBM in OSA. The short-term goal of this project is to collect pilot data, which is the first of its kind, and suggest tPBM as a potential modulator of sleepiness in OSA.
Conditions Studied
Interventions
- DEVICE Active tPBM
Study Locations (1)
New York
- NYU Langone Health - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 22 participants |
| Start Date | 2026-01-12 |
| Est. Completion | 2026-10-03 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06698809
The ClinicalTrials.gov registry entry for NCT06698809 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 22 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 221-participant average among 155 other Obstructive Sleep Apnea trials with a reported enrollment target (90% lower). The listed sponsor is NYU Langone Health, which has 1,164 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 Active tPBM is the first listed.
NCT06698809 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT06698809 about?
NCT06698809 is a clinical study titled "Obstructive Sleep Apnea Therapeutic Intervention for REsiDual Sleepiness". Obstructive sleep apnea (OSA) is a sleep disorder that is commonly treated using positive airway pressure, yet 50% of patients still experience residual sleepiness after successful therapy. A potential neuromodulation strategy that can decrease residual sleepiness is transcranial photobiomodulation ...
What is the current status of trial NCT06698809?
This trial is currently recruiting. It is a NA study. The enrollment target is 22 participants. The study started on 2026-01-12. Estimated completion is 2026-10-03.
What conditions does trial NCT06698809 study?
This clinical trial studies the following conditions: Obstructive Sleep Apnea, Sleepiness.
What interventions are being tested in trial NCT06698809?
The interventions under investigation include: Active tPBM (DEVICE).
Who is sponsoring clinical trial NCT06698809?
This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06698809 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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