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Study details
Enrolling now

Obstructive Sleep Apnea Therapeutic Intervention for REsiDual Sleepiness

NYU Langone Health
NCT IDNCT06698809ClinicalTrials.gov data as of Apr 2026
Target enrollment

18

Study length

about 7 months

Ages

18–75

Locations

1 site in NY

What this study is about

This trial is testing if transcranial photobiomodulation (tPBM) can help reduce residual sleepiness in people with obstructive sleep apnea. tPBM uses red and near-infrared light to potentially change brain activity and blood flow, which may improve sleepiness.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Use Active tPBM

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.