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AI-Designed Clear Aligners: A Randomized Clinical Trial

Clinical Performance of AI-based TruRoot Designed Clear Aligner (A Randomized Clinical Trial)

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06968325
Enrollment
40
Registered
2025-05-13
Start date
2025-02-25
Completion date
2026-12-01
Last updated
2025-05-21

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

Conditions

Pain Perception, Root Resorption, Treatment Duration

Keywords

Clear aligners Orthodontics Artificial intelligence Root positioning CBCT Intraoral scan TruRoot Segmentation

Brief summary

The goal of this clinical trial is to evaluate the clinical performance and validity of applying AI-based TruRoot-designed clear aligners in adult orthodontic patients. The main questions it aims to answer are: Do TruRoot-designed aligners achieve more accurate root positioning compared to conventional aligners? Is there a significant difference in clinical parameters such as root resorption, pain levels, treatment duration, and occlusal outcomes between the two groups? Is the TruRoot AI-based design a valid and clinically applicable method for planning clear aligner treatment? Researchers will compare: An AI-based TruRoot group, where aligners are planned using CBCT and intraoral scan superimposition to estimate true root position A Conventional group, where aligners are designed using intraoral scans only, with expert evaluation to ensure roots remain within the alveolar bone Participants will: Receive clear aligner treatment based on either the TruRoot AI system or conventional planning by experts Undergo CBCT and intraoral scans at baseline and post-treatment Be assessed for root position accuracy, validity of AI-generated treatment plans, occlusal outcomes via the ABO Objective Grading System, root resorption, self-reported pain, and treatment duration Attend regular follow-ups throughout the treatment period

Detailed description

This randomized clinical trial investigates the clinical validity and performance of AI-based TruRoot-designed clear aligners compared to conventionally designed clear aligners in adult patients undergoing orthodontic treatment. The TruRoot system integrates CBCT and intraoral scan superimposition to estimate true root positioning, whereas the conventional group relies solely on intraoral scans with manual verification by expert orthodontists to ensure root positioning within the alveolar bone. The primary aim is to assess whether AI-driven root-based treatment planning offers superior clinical outcomes in terms of root accuracy, treatment efficiency, root resorption, pain perception, and occlusal quality. Post-treatment assessments will include CBCT imaging, root position analysis, and occlusal outcome evaluation using the American Board of Orthodontics (ABO) Objective Grading System. A comprehensive digital workflow will be applied throughout the study: CRANEX® software will be used for generating high-resolution CBCT slice data. BlueSky Plan or AI-based CephX® Web Viewer will be employed for segmentation and 3D modeling of dental and skeletal structures. Clear aligner designs will be generated through BlueSky Plan software or 3Shape Clear Aligner Studio, incorporating the AI-based TruRoot protocol in the experimental group. OnDemand 3D software will be used to evaluate root positioning within the alveolar bone post-treatment. Geomagic® Control X™ will be utilized to quantify tooth movement and assess root volume changes throughout the treatment course. This study will generate clinical data to validate the use of AI-powered root-based planning protocols in aligner therapy and compare them to conventional expert-driven methods

Interventions

DEVICEAI-based TruRoot group:

Participants in this group will receive clear aligner treatment designed using an artificial intelligence (AI)-based system called TruRoot

DEVICEConventional clear aligner group

Participants in this group will receive clear aligner treatment planned manually by expert orthodontists based only on intraoral scans.

Sponsors

University of Baghdad
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
No

Inclusion criteria

1. All participants should have good general health with healthy periodontium. 2. Adult patient with an age range 18-30 with fully erupted all permanent dentitions excluding third molars. 3. Skeletal and dental Cl I malocclusion with moderate crowding (little irregularity index 4-6 mm). 4. The treatment plan should be non-extraction treatment. 5. No history of trauma or root resorption

Exclusion criteria

1. Patients with diseases or syndromes affecting maxillofacial regions, 2. Subject with poor oral hygiene. 3. Defective and missing teeth. 4. Presence of any deep bite or open bite problems, 5. History of trauma, root resorptions and dilacerated roots. 6. Medical conditions affecting tooth movement or bone metabolism. 7. previous extraction or history of previous orthodontic treatment.

Design outcomes

Primary

MeasureTime frameDescription
Root position and movementat the end of treatmentAssessment of the accuracy of final root positions relative to the planned positions in both groups after applying certain amount of torque. and
Assessment of Root Position Relative to Alveolar Bonebefore treatment beginEvaluation of whether the initially planned root positions in the conventional clear aligner group are contained within the alveolar bone. The assessment will be performed by importing the final STL model (planned before treatment) and superimposing it with pre-treatment CBCT scans.

Countries

Iraq

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026