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Terminated Not applicable Interventional Results available

A Study to Compare Nighttime Aligners to Daytime Aligners

ClinicalTrials.gov ID: NCT06539676

Public ClinicalTrials.gov record NCT06539676. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 7:39 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective, Two-armed, Multicenter Clinical Study to Evaluate Efficacy, Performance, and Safety of Nighttime Aligners (Worn 10-12 Hours Day or Night) Compared to Daytime Aligners (Worn 20-22 Hours Day/Night)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this research study is to see if Nighttime Aligners (worn 10-12 hours per day or night) are effective and safe for tooth movement and if so, how they compare with the standard Daytime aligners (worn 20-22 hours per day), in adults and children from 12 years of age and older. It will investigate the efficacy and performance of the treatments, as well as the safety of the investigational device and comparator. The main objectives are: * Comparison between the two groups concerning actual vs planned tooth movements (measured by changes in tooth position) * Comparison between the two groups concerning the incidence of device or dental related AEs. * Overall dentist and participant satisfaction with the treatment. Participants will: * Be given orthodontic aligner therapy with the Daytime (20-22h/day) or Nighttime (10-12h/day) Aligners (randomly assigned) * Attend approximately 5 study during approximately 8-10 months

Study identification

NCT ID
NCT06539676
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Enrollment
7 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 3, 2024
Primary completion
Jan 16, 2025
Completion
Jan 16, 2025
Last update posted
Jul 15, 2025

2024 – 2025

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Fulbright Dental Redondo Beach California 90277
3D Dental Miami Beach Florida 33140
Elite Dental of Towson Towson Maryland 21204
Cedars Family Dental Plainville Massachusetts 02762
R. Lobato & Associates Las Vegas Nevada 89117
Aesthetic Dental North Bergen New Jersey 07047
Huerta Dentistry New York New York 10001
Brush365 Frisco Texas 75035
Gustafson Dental Humble Texas 77396
SKM Dentistry d/b/a brush365 Dental Hurst Texas 76003
Northwest Dental Medicine Puyallup Washington 98372
Gregson Family Dentistry Milwaukee Wisconsin 17655

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06539676, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 15, 2025 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06539676 live on ClinicalTrials.gov.

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