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NCT Number: NCT07220317

This Study Will Examine Shortened Treatment Wear Time for Patients With Mixed Dentition Using AirFlex Aligner, Sequential Dental Aligners.

This study will examine shortened treatment wear time for patients with mixed dentition using sequential dental aligners. Using the existing AirFlex aligner design that patients with permanent dentition use, it may be possible to reduce the wear time and still provide dental realignment in an adequate treatment period for patients with mixed dentition. The Airflex aligner will be tested for a 9-12-hour patient wear time.

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Key information

Age range

7 year–21 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

The primary intervention is the change in active wear time. In current practice, sequential aligners are prescribed to be worn approximately 20 to 22 hours per day. In this study, the prescribed wear time will be reduced to 9 - 12 hours per day.

This study is intended to demonstrate effectiveness of AirFlex aligners, which have a reduced wear time compared to traditional aligners, in mixed dentition subjects. The study will be conducted using AirFlex aligners, which are currently cleared for treatment of patients with permanent dentition.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Male or female, aged 7 to 21 years old
  • Mixed dentition, as defined by the presence of at least one primary tooth present at the start of orthodontic treatment
  • No untreated cavities
  • Good Periodontal composition as determined by dental exam

Exclusion criteria

  • Skeletal discrepancies requiring surgery
  • Is currently undergoing dental/orthodontic work
  • Has dental prosthesis/implants that will interfere with projected tooth movement
  • Ongoing use of medication affecting tooth movement or bone formation (NSAIDS, Steroids, Bisphosphonates, Levothyroxine, Teriparatides, etc.)
  • Is currently pregnant or plans to become pregnant during treatment
  • Current smoker or tobacco use within 2 years
  • Presence of systemic diseases that could interfere with treatment
  • Moderate or significant periodontal disease
  • Any other physical exam finding that precludes participation

Treatment and study plan

Sequential Aligners

Device

Treatment with sequential aligners in a shortened wear time with mixed dentition.

Primary outcomes

  1. The primary endpoint will assess the tooth movements (torque, extrusion, rotation, translation, intrusions, and tipping), ensuring that final dentition is within 0.3 mm of the intended position.

    Time frame: 16 weeks

Sponsors and collaborators

Lead sponsor

OrthoFX

Industry

Registry information

Official study title

A Clinical Evaluation of Orthodontic Tooth Movements in Mixed Dentition

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Oct 23, 2025
Registry last updated
Oct 23, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.