Recruiting at 1 site No phase Pediatric Obstructive Sleep Apnea

Clinical trial for Pediatric Obstructive Sleep Apnea

Official title Pediatric Down Syndrome Post-Approval Study

ClinicalTrials.gov ID: NCT06851338

What this study is testing

What it's testing
The study aims to see if the Inspire therapy remains safe and effective for young people with Down syndrome who have severe sleep apnea.
Who it's for
The study is looking for adolescents and young adults aged 13 to 18 who have Down syndrome and severe sleep apnea.
What's involved
Participants will use the Inspire therapy, which is a device that helps keep the airway open during sleep, and undergo regular check-ups to monitor their health.
Time commitment
The study involves ongoing monitoring to track safety and effectiveness over time.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 13 to 18

You may be able to join if

  • Patient has been diagnosed with Down syndrome;
  • Patient is 13-18 years of age;
  • Patient has been diagnosed with severe obstructive sleep apnea, with an AHI of ≥ 10 and ≤ 50 based on a recent (within 6 months of enrollment)...
  • Patient has documented failure of, or intolerance to, positive airway pressure therapies (such as CPAP or BiPAP) despite attempts to improve...
  • Patient is contraindicated for, or not effectively treated by, adenotonsillectomy;

You likely can't join if

  • Patient's recent PSG (within 6 months of enrollment) reports central + mixed apneas \> 25% of the total apnea-hypopnea index (AHI);
  • Patient has any anatomical finding that would compromise the performance of upper airway stimulation, such as the presence of complete concentric...
  • Patient has any condition or procedure that has compromised neurological control of the upper airway;
  • Patient, or their parent/guardian, is unable or does not have the necessary assistance to operate the patient remote;
  • Patient is pregnant or plans to become pregnant;
  • Patient has an implantable device that may be susceptible to unintended interaction with the Inspire system;
See the full eligibility criteria
Who can join
  • Patient has been diagnosed with Down syndrome;
  • Patient is 13-18 years of age;
  • Patient has been diagnosed with severe obstructive sleep apnea, with an AHI of ≥ 10 and ≤ 50 based on a recent (within 6 months of enrollment) qualified in-lab sleep study (PSG);
  • Patient has documented failure of, or intolerance to, positive airway pressure therapies (such as CPAP or BiPAP) despite attempts to improve compliance;
  • Patient is contraindicated for, or not effectively treated by, adenotonsillectomy;
  • Treatment of patient's OSA has followed standard of care in considering all other alternative/adjunctive therapies;
  • Patient, and their parents/guardians, is willing to have stimulation hardware permanently implanted, and be willing to participate in follow-up visits, postoperative in-lab sleep studies (PSGs), and questionnaire...
What rules you out
  • Patient's recent PSG (within 6 months of enrollment) reports central + mixed apneas \> 25% of the total apnea-hypopnea index (AHI);
  • Patient has any anatomical finding that would compromise the performance of upper airway stimulation, such as the presence of complete concentric collapse of the soft palate;
  • Patient has any condition or procedure that has compromised neurological control of the upper airway;
  • Patient, or their parent/guardian, is unable or does not have the necessary assistance to operate the patient remote;
  • Patient is pregnant or plans to become pregnant;
  • Patient has an implantable device that may be susceptible to unintended interaction with the Inspire system;
  • Patient will require magnetic resonance imaging (MRI) other than what is specified in the MR conditional labeling;
  • Patient has a terminal illness with life expectancy of less than 12 months;
  • Any other reason the investigator deems the patient is unfit for participation in the study.

The study team makes the final eligibility decision.

Where it is enrolling

  • Houston, Texas, United States

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part, but confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 13 years to 18 years. The study team makes the final eligibility decision.

Where is this trial taking place?

This study is enrolling now at Houston, Texas, United States. Enter your location above to see the nearest enrolling site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool that is independent of the study sponsor. Details come from ClinicalTrials.gov. The study team decides eligibility, and your own doctor gives medical advice.