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Study identifier: NCT06655844 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Sana Device for Post-Treatment Lyme Disease Syndrome Chronic Pain

Condition: Post-treatment Lyme Disease Syndrome · Chronic Pain  ·  Sponsor: Icahn School of Medicine at Mount Sinai

PhaseNA
Planned participants20
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study will investigate the effectiveness of the Sana Pain Reliever (Sana PR) at reducing chronic pain. The Sana PR is a device comprised of one main component (Mask with Earbuds) and two ancillary components (Charger and Headband). The device is worn over the eyes (with earbuds in ears). The device pulses light at a single wavelength but various frequencies throughout a specific firmware algorithm. Through the earbuds, the device also plays different tones in conjunction with the pulses. The device has a skin contacting Heart Rate Variability (HRV) sensor built into the forehead area that measures HRV throughout the use of the device. The system runs for 15 min at a time and is not FDA approved. The trial will last a total of 14 weeks. 50 participants who have a diagnosis of Post-treatment Lyme Disease and experience chronic pain are expected to take part in this study at Mount Sinai.

This description comes directly from the study's public registry record.

Talk to the study team

Laura Tabacof, MD  ·  212-241-8454  ·  CoreResearch@mountsinai.org

Always discuss trial participation with your own doctor first.

Locations (1)

The Cohen Center for Recovery from Complex Chronic Illnesses (CoRE)New York, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06655844