Actively Recruiting

All Genders
Healthy Volunteers
NCT07261735

Clinical Evaluation of Customized Attachment Composites in Clear Aligner Therapy

Led by Saglik Bilimleri Universitesi · Updated on 2026-04-30

24

Participants Needed

1

Research Sites

48 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This prospective observational clinical study aims to evaluate the three-dimensional surface wear and clinical survival of orthodontic attachments fabricated with customized composite materials used in clear aligner therapy. Attachments play a critical role in the biomechanical efficiency of aligner treatment by facilitating planned tooth movements. However, the mechanical and surface properties of the composites used for attachment fabrication may affect their wear behavior and long-term stability. In this study, four different composite materials will be tested using a split-mouth design in patients treated with clear aligners. Each quadrant will receive a different composite, including both customized and universal types. All attachments will be fabricated using standardized digital templates and bonded under identical clinical conditions. Surface wear will be evaluated using three-dimensional optical scanning and metrology software at baseline, 1 week, 1 month, 3 months, and 6 months. Lost attachments will be replaced and recorded but excluded from wear analysis. The results of this study are expected to provide valuable insights into the optimal material selection for clear aligner attachments, improving treatment accuracy and clinical durability.

CONDITIONS

Official Title

Clinical Evaluation of Customized Attachment Composites in Clear Aligner Therapy

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Fully erupted permanent dentition
  • No existing prosthetic restorations
  • Mild-to-moderate dental crowding or spacing (2-6 mm)
  • Scheduled to undergo clear aligner therapy at the Department of Orthodontics, Gülhane Faculty of Dentistry, between 01.08.2025 and 01.08.2026
  • Agree to participate and provide informed consent
Not Eligible

You will not qualify if you...

  • History of previous fixed orthodontic treatment
  • Poor predicted compliance or low cooperation
  • Presence of severe or generalized periodontal disease
  • High caries incidence or untreated caries
  • Poor oral hygiene
  • Habitual consumption of hard foods
  • Bruxism
  • Congenitally missing permanent teeth
  • Dental developmental anomalies
  • Teeth with existing composite resin restorations or ceramic crowns on buccal surfaces that may interfere with bonding or wear analysis

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of Health Sciences, Gülhane Faculty of Dental Medicine

Ankara, Turkey (Türkiye)

Actively Recruiting

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Research Team

G

Gizem Boztaş Demir, Asst. Prof.

CONTACT

K

Kübra Gülnur Topsakal, Assoc. Prof. Dr.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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