Otolaryngological Disease study: DISE-Directed Surgery vs Adenotonsillectomy
Official title Treatment of Obstructive Sleep Apnea With Personalized Surgery in Children With Small Tonsils
ClinicalTrials.gov ID: NCT06258837
What this study is testing
- What it's testing
- The study compares a new personalized surgical plan, guided by a sleep endoscopy, to the usual tonsil removal. It aims to see if the personalized approach gives better results after six months.
- Who it's for
- Children aged 2 to 17 who have small tonsils and obstructive sleep apnea.
- What's involved
- Participants will be randomly assigned to either the personalized surgery or the standard tonsil removal. They will have the chosen procedure and follow-up visits to assess outcomes.
- Time commitment
- The study lasts six months, with visits before and after the surgery to monitor progress.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 2 to 17
You may be able to join if
- Child has a diagnosis of moderate to severe OSA diagnosed by PSG (oAHI ≥ 5).
- Child age is 2.00 to 17.99 years of age.
- Child has small tonsils (Brodsky 1+ or 2+) noted during routine physical exam.
- Caregiver can provide signed and dated consent and is 18 years of age or older at the time of consent.
- Caregiver can speak, read, and write in English or Spanish.
See the full eligibility criteria
- Child has a diagnosis of moderate to severe OSA diagnosed by PSG (oAHI ≥ 5).
- Child age is 2.00 to 17.99 years of age.
- Child has small tonsils (Brodsky 1+ or 2+) noted during routine physical exam.
- Caregiver can provide signed and dated consent and is 18 years of age or older at the time of consent.
- Caregiver can speak, read, and write in English or Spanish.
- Caregiver is primary caretaker of the child.
- Child is not expecting their own child.
- Child has history of previous tonsillectomy, tonsillotomy, or partial tonsillectomy.
- Child has any contraindication to surgery (e.g. bleeding disorders).
- Child has significant cardiopulmonary comorbidity besides OSA requiring supplemental oxygen, subglottic or tracheal stenosis, tracheostomy dependence.
- Child has a genetic abnormality, Down syndrome, neuromuscular disorder, craniofacial anomaly.
- Caregiver is unwilling or unable to comply with study procedures.
- Child is or plans to become a parent themselves.
The study team makes the final eligibility decision.
Where it is enrolling
- Ann Arbor, Michigan, United States
- Portland, Oregon, 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, 2 years to 17 years. The study team makes the final eligibility decision.
Where is this trial taking place?
This study is enrolling now at Ann Arbor, Michigan, United States; Portland, Oregon, 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.