Trial · NCT07902908
Use of a Mandibular Advancement Appliance in Children With Obstructive Sleep Apnea
NCT07902908, Not applicable, Not yet recruiting, National Institute of Dental and Craniofacial Research (NIDCR)
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Use of a Mandibular Advancement Appliance in Children With Obstructive Sleep Apnea. Trials, record NCT07902908. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07902908
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Use of a Mandibular Advancement Appliance in Children With Obstructive Sleep Apnea
- NCT number
- NCT07902908
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 25 participants, estimated
- Lead sponsor
- National Institute of Dental and Craniofacial Research (NIDCR)
- Conditions
- Obstructive Sleep Apnea (OSA), Pediatric Obstructive Sleep Apnea (OSA), Adeno-Tonsillar Hypertrophy, Maxillary Hypoplasia, Mandibular Hypoplasia, Obesity, Intraoral Appliance
- Interventions
- DynaFlex Dorsal Accu-Fit
- First posted
- 2026-10-29
- Last updated
- 2026-11-12
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | The primary objective of this study is to determine the adherence levels, the safety, and the preliminary efficacy of this anterior mandibular repositioning appliance in the management of OSA in children. | 5 months. | \- The number of nights that the patient has been wearing the appliance per week.- Number and type of associated adverse events reported during the trial.- The pre- and post-intervention change in the Apnea Hypopnea Index (AHI) |
| Secondary | The evaluation of the potential impact of the use of the appliance on the morphology of the nasopharyngeal airway. | 4 months. | Assessment of the changes in the airway volume and minimal axial sections areas with the use of a pre- and post-treatment CBCT scan. |
| Secondary | The evaluation of the impact of the use of the appliance on craniofacial skeletal relationships. | 4 months. | Detailed clinical and radiographic craniofacial evaluation of pre- and post-treatment dental and skeletal tissue relationships with the use of clinical records and CBCT scan images. |
| Secondary | The potential changes in the symptoms associated with OSA pre- and post-intervention. | 4 months. | The scores in the Pediatric Sleep Questionnaire (PSQ) pre- and post-intervention will be compared. |
| Secondary | The changes in the quality of life of the participants. | 4 months. | The scores in the OSA-18 questionnaire pre- and post-intervention will be compared. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07902908
GET https://conductscience.org/api/trials/v1/NCT07902908/registered