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Completed

NCT Number: NCT06685029

A Comparison of Direct 3D Printed Clear Aligner System and Indirect Clear Aligner Systems With Fixed Orthodontic Treatment in Terms of Endocrine Disrupting Monomer Release, Treatment Effectiveness and Efficiency

The aim of this study is to evaluate the release of endocrine disrupting monomers from clear aligners as a result of exposure to intraoral factors by measuring their concentration in saliva and to evaluate their reliability of use in terms of general health by comparing them with the fixed orthodontic treatment group. It is also aimed to compare the groups in terms of treatment effectiveness and efficiency.

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Key information

Age range

15 year–24 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Erciyes University,Faculty of Dentistry,Department of Orthodontics

Kayseri, 38000, Turkey (Türkiye)

About this study

The aim of our study is to evaluate the saliva concentration of endocrine-disrupting monomers released from attachments used and clear aligners produced directly by the orthodontist in the clinic and indirectly produced by companies. Accordingly comparing them with the fixed orthodontic treatment group and assessing clear aligner's safety for general health. It is also aimed to compare the groups in terms of treatment effectivenes and total time spent . Endocrine-disrupting chemicals are substances that interfere with the synthesis, metabolism, or effects of hormones, causing deviation from normal reproduction and homeostatic control in organisms. Bisphenol A (BPA), a monomer, is also included in the chemicals listed as endocrine disruptors by the World Health Organization. Different studies have suggested that Bisphenol A may cause adverse health effects by acting as an endocrine disruptor. While previous research has been conducted on BPA release or monomer leakage related to orthodontic materials, there is limited evidence regarding the safety aspects of thermoplastic aligners or retainers. The concentrations of endocrine-disrupting monomers in the saliva of patients undergoing treatment with directly produced aligners by orthodontists and indirectly produced aligners by companies will be examined in comparison to patients undergoing fixed orthodontic treatment. Patients will not receive any treatment other than routine orthodontic care.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Absence of primary teeth in the oral cavity, with permanent teeth fully erupted,
  • Presence of a non-extraction orthodontic treatment plan,
  • Age range of 15 to 24 years,
  • Presence of mild to moderate dental crowding (0-6 mm of crowding),
  • Classification as skeletal Class I (ANB: 2±2°),
  • Absence of any craniofacial anomalies,
  • Normal vertical growth pattern (Sn-GoGn: 32±6°),
  • No congenital tooth agenesis (excluding third molars),
  • Absence of atypical tooth morphology,
  • No extracted permanent teeth,
  • Absence of dental caries,
  • Good level of oral hygiene,
  • Healthy periodontal tissues.

Exclusion criteria

  • Presence of any systemic disease,
  • History of previous fixed orthodontic treatment,
  • History of allergy to any dental material,
  • Use of medications containing estrogen analogs,
  • Patients with a history of xerostomia and a salivary flow rate of less than 0.1 ml per minute,
  • Patients with more than five composite restorations.

Treatment and study plan

Clear Aligner treatment

Device

Clear aligners are appliances that allow the teeth to be gradually moved to the desired final position, as planned in the computer program, in a way that each aligner will perform a part of the total movement with its use.

Fixed Orthodontic Appliance Treatment

Device

Fixed orthodontic treatment is a type of orthodontic treatment performed by applying brackets and wires to the teeth and is considered the gold standard for orthodontic treatments.

Primary outcomes

  1. Bisphenol A Concentration

    Time frame: up to 1 year

    Bisphenol A concentration in patients' saliva is measured as ng/ml.

Secondary outcomes

  1. Treatment efficiency

    Time frame: up to 1 year

    The total time required to complete the treatment is calculated.

  2. Treatment Effectiveness (via PAR İndex)

    Time frame: up to 1 year

    The percentage decrease in the PAR score is calculated for each group.

Sponsors and collaborators

Lead sponsor

Ahmet Yağcı

Other

Registry information

Official study title

Comparison of Clear Aligner System Produced Directly by the Orthodontist and Indirect Clear Aligner Systems With Fixed Orthodontic Treatment in Terms of Endocrine Disrupting Monomer Release: In-vivo Randomized Controlled Clinical Study

Important dates

Study start
2023
Primary completion
2024
Study completion
2025
First posted
Nov 12, 2024
Registry last updated
Sep 25, 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.

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