Skip to content

Clinical Trial to Assess the Efficacy of Reducing the Aligners' Wear Protocol

A Randomized Clinical Trial to Assess the Efficacy of Reducing the Aligners' Wear Protocol on the Predictability of Orthodontic Tooth Movement

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05905224
Enrollment
40
Registered
2023-06-15
Start date
2023-10-30
Completion date
2026-02-28
Last updated
2026-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Orthodontic Tooth Movement

Keywords

clear aligners, wear protocol, 3-day wear, 7-day wear, rate and amount of tooth movement, accuracy, outcomes

Brief summary

The hypothesis of this project is that replacing the current 7-day wear protocol with a 3-day wear protocol, while integrating less tooth movement per aligner (reduce the amount of activation per aligner) may produce more consistent and continues orthodontic forces, therefore, increase the predictability, accuracy and outcomes achieved for various types of tooth movements and enhance the rate of tooth movement with the Invisalign system

Detailed description

This randomized clinical trial aims to assess the effectiveness of increasing the frequency of change per aligner, within the standard of care, on the efficacy of achieving better treatment outcomes. We will study the influence of reducing the wear scheduled for Invisalign clear aligners, from 7-day change per aligner to 3-day change per aligner, on the predictability and accuracy of different orthodontic tooth movements by comparing the simulated predicted final outcomes to those achieved at the end of treatment between the two change protocols.

Interventions

DEVICEInvisalign 7-day wear protocol

Clear Aligners' (Invisalign, Align technology, San Jose, Calif) 7-day wear protocol

DEVICEInvisalign 3-day wear protocol

Clear Aligners' (Invisalign, Align technology, San Jose, Calif) 3-day wear protocol

Sponsors

University of Florida
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Physically healthy with no relevant allergies or medical problems * Male or female between the age of 18 and 30. * Full permanent dentition except for the third molars * Class I crowded dentition primarily for the lower anterior teeth (moderate crowding - 4-6 mm - according to Little's Irregularity Index) * Good oral hygiene and absence of periodontal disease * Malocclusion to be treated with Invisalign aligners (SmartTrack) * Any ethnic group

Exclusion criteria

* Orthognathic surgical cases * An extraction treatment plan * Poor oral hygiene * Patients with syndromes or craniofacial anomalies. * The use of any other orthodontic appliance than clear aligners' (Invisalign)

Design outcomes

Primary

MeasureTime frameDescription
predictability of the different orthodontic tooth achieved in each of the studies groups movements achieved at the end of treatment in each of the studied groups (3-day wear vs 7-day wear).14 monthsassess the influence of reducing the wear scheduled for Invisalign clear aligners, from 7- day wear to 3-day wear, on the predictability and accuracy of different orthodontic tooth movements by comparing the simulated predicted final outcomes to those achieved at the end of treatment between the two wear protocols.
rate of tooth movement for the lower anterior teeth as detected by the consecutive scans captured by the scan box (Dental Monitoring®) in the first 8 weeks of treatment2 monthscompare and quantify the magnitude and rate of orthodontic tooth movement between the suggested (3-day) and conventional (7-day) wear protocols for the Invisalign® system using the Dental Monitoring superimposed scans and the data collected from their online platform in the first 8 weeks after Invisalign delivery.

Secondary

MeasureTime frameDescription
duration of treatment14 monthsthe total time needed to complete treatment
number of refinements and visits needed for each wear protocol.14 monthsthe number of additional mid adjustment treatment scans needed for each included subject during the clinical trial duration
Occlusal outcomes14 monthsThe Peer Assessment rate and/or ABO grading system will be used to measure the final occlusal outcomes achieved in both groups for them to be compared.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORSarah Abu Arqub, DDS

University of Florida

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 7, 2026