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NCT06539676 · ClinicalTrials.gov registry record · NA

A Study to Compare Nighttime Aligners to Daytime Aligners

A NA study, sponsored by Dentsply Sirona Implants and Consumables.

Terminated
Registry status
NA
Development phase
7
Enrollment target

NCT06539676 is a NA study that was terminated before completion, run by Dentsply Sirona Implants and Consumables. The registered enrollment target is 7 participants.

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The verdict

NCT06539676, a NA study, was terminated before completion, sponsored by Dentsply Sirona Implants and Consumables.

TERMINATED
Registry status
NA
Development phase
7 participants
Enrollment target

Study Summary

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

Interventions

  • DEVICE Nighttime Aligners
  • DEVICE Daytime Aligners

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2024-09-04
Est. Completion 2025-01-17
Phase NA

What the Registry Record Tells You About NCT06539676

The ClinicalTrials.gov registry entry for NCT06539676 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 7 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Dentsply Sirona Implants and Consumables, which has 24 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Nighttime Aligners is the first listed.

NCT06539676 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT06539676 about?

NCT06539676 is a clinical study titled "A Study to Compare Nighttime Aligners to Daytime Aligners". 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 ...

What is the current status of trial NCT06539676?

This trial is currently terminated. It is a NA study. The enrollment target is 7 participants. The study started on 2024-09-04. Estimated completion is 2025-01-17.

What interventions are being tested in trial NCT06539676?

The interventions under investigation include: Nighttime Aligners (DEVICE), Daytime Aligners (DEVICE).

Who is sponsoring clinical trial NCT06539676?

This trial is sponsored by Dentsply Sirona Implants and Consumables, which has 24 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.