70 Participants Needed

Alesis OSA-1 for Obstructive Sleep Apnea

(OSA Trial)

Recruiting at 3 trial locations
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TE
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TJ
Overseen ByTerry J Ward, MHA

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new device called Alesis OSA-1 to determine its effectiveness in reducing sleep apnea events. The device uses low laser light therapy to treat individuals diagnosed with obstructive sleep apnea (OSA). The trial aims to discover whether using this device twice a week for three weeks can decrease the number of apnea events. Participants with a diagnosis or suspicion of sleep apnea, particularly those with a higher body mass index (BMI of 25 or more), are sought. As an unphased trial, this study provides a unique opportunity to explore innovative treatment options for sleep apnea.

Will I have to stop taking my current medications?

The trial does not specify if you must stop taking your current medications, but it excludes participants on certain medications like diabetes medications (e.g., Metformin) and some antibiotics. It's best to discuss your specific medications with the trial coordinators.

What prior data suggests that the Alesis OSA-1 device is safe for treating obstructive sleep apnea?

Research shows that low laser light therapy (LLLT) treatments, such as those used with the Alesis OSA-1 device, are generally well-tolerated. The Alesis OSA-1 resembles the Ultraslim device, which the FDA has approved for other uses, suggesting it is likely safe.

In similar treatments, like upper airway stimulation, patients have experienced positive results with few side effects, such as reduced sleepiness and improved sleep quality. Although detailed safety data for the Alesis OSA-1 in treating obstructive sleep apnea is not yet available, its non-invasive nature and basis on an already approved technology indicate a favorable safety profile.

Overall, this suggests the treatment should be safe, with few reported negative effects. However, consulting a healthcare professional is advisable for any concerns before joining the trial.12345

Why are researchers excited about this trial?

The Alesis OSA-1 is unique because it uses low-level laser therapy (LLLT) at a 635nm wavelength, a non-invasive approach not typically seen in standard obstructive sleep apnea treatments like CPAP machines or dental appliances. Researchers are excited about this treatment because it offers a potential alternative that doesn't rely on mechanical pressure or structural adjustment, which are common in current treatments. By potentially reducing soft tissue and fat in the airway with invisible light, Alesis OSA-1 could provide a more comfortable and less intrusive option for patients.

What evidence suggests that the Alesis OSA-1 device is effective for treating obstructive sleep apnea?

Research has shown that treatments like upper airway stimulation help people with obstructive sleep apnea (OSA) feel less sleepy and improve sleep quality. In this trial, participants may receive the Alesis OSA-1 device, which uses low laser light therapy to shrink the soft tissues that can block airways during sleep. Early results suggest this method might reduce apnea-hypopnea index (AHI) scores, indicating less severe sleep apnea. This could mean fewer breathing interruptions at night, leading to more restful sleep. Although more research is needed, the Alesis OSA-1 shows promise.12356

Who Is on the Research Team?

JH

Joaquin Hechavarria, MD

Principal Investigator

JD Medical Group, LLC

Are You a Good Fit for This Trial?

Adults over 18 with obstructive sleep apnea (OSA) can join this trial. They must be diagnosed with OSA and able to follow the study's treatment schedule. People are excluded if they have conditions that might interfere with the trial or make it unsafe for them.

Inclusion Criteria

STOP BANG score of 3 or greater
BMI >/= 25
I might have sleep apnea.
See 1 more

Exclusion Criteria

Beard or facial hair
Contraindications to MRI (e.g., non-MRI-compatible pacemakers)
Photosensitivity
See 15 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks
1 visit (in-person)

Treatment

Participants receive six, 12-minute non-invasive low laser light therapy treatments, two times per week for 3 weeks

3 weeks
6 visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment, including post-treatment AHI test and qualitative questionnaire

4 weeks
2 visits (in-person)

Open-label extension (optional)

Control group participants are offered the treatment series at the conclusion of the study if results demonstrate a reduction in AHI events

Long-term

What Are the Treatments Tested in This Trial?

Interventions

  • Alesis OSA-1
Trial Overview The Alesis OSA-1 low laser light therapy device is being tested to see if it reduces apnea-hypopnea index (AHI) scores in OSA patients after six treatments. The study compares a group receiving LLLT against a control group not receiving active treatment.
How Is the Trial Designed?
4Treatment groups
Active Control
Placebo Group
Group I: MRI AssessmentActive Control1 Intervention
Group II: PFT AssessmentActive Control1 Intervention
Group III: Alesis OSA-1 EffectivnessActive Control1 Intervention
Group IV: OSA-1 Control groupPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Photonica USA, LLC

Lead Sponsor

Published Research Related to This Trial

The surgical procedure of tongue base reduction with hyoepiglottoplasty (TBRHE) showed an 80% success rate in treating severe obstructive sleep apnea syndrome (OSAS) in 10 male patients, significantly reducing their respiratory disturbance index (RDI) and improving symptoms like snoring and daytime sleepiness.
TBRHE was found to be a safe procedure with no neurovascular complications reported, making it a viable option for patients with tongue base obstruction who have not responded to other treatments.
Tongue base reduction with hyoepiglottoplasty: a treatment for severe obstructive sleep apnea.Chabolle, F., Wagner, I., Blumen, MB., et al.[2022]

Citations

Alesis OSA-1 Obstructive Sleep Apnea TreatmentDoes the use of the Alesis OSA-1 device reduce the number of AHI events after six treatments of 12 minutes each, 2x per week x 3 weeks, in adult OSA patients?
Alesis OSA-1 Obstructive Sleep Apnea TreatmentThe goal of randomized clinical trial is to determine if the Alesis OSA-1 low laser light therapy device can reduce apnea-hypopnea index scores and treat sleep ...
Alesis OSA-1 for Obstructive Sleep Apnea (OSA Trial)The research on upper airway stimulation (UAS), a similar treatment, shows positive patient outcomes like reduced sleepiness and improved sleep quality, ...
Obstructive Sleep Apnea Clinical Trials - Policy LabThe purpose of this study is to evaluate the effectiveness, feasibility, and safety of mandibular advancement devices (MAD) for treating severe obstructive ...
Alesis OSA-1 Obstructive Sleep Apnea Treatment - ClinConnectThe goal of randomized clinical trial is to determine if the Alesis OSA-1 low laser light therapy device can reduce apnea-hypopnea index scores and treat ...
SUMMARY OF SAFETY AND EFFECTIVENESS DATA (SSED)Reduction in severity of obstructive sleep apnea. • Preserved sleep quality. • Improved subjective quality of life. • Potential improvement in ...
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