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Surface Wear of Clear Aligner Attachment Composites

Evaluation of Surface Wear of Composites Used for Clear Aligner Attachments

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07812220
Enrollment
35
Registered
2026-09-10
Start date
2024-12-24
Completion date
2026-07-23
Last updated
2026-09-10

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

Conditions

Clear Aligner Therapy, Composite Resins

Keywords

surface wear, volume loss, clear aligner attachments, flowable composite

Brief summary

The aim of this study is to investigate the amount of surface wear that may occur during treatment with different composite materials used for clear aligner attachments. Two different flowable composites (AlignerFlow LC, VOCO GmbH, Cuxhaven, Germany; AlignerConnect, GC, Tokyo, Japan) will be used to bond the attachments in split mouth designs. To determine the composite for the upper right segment, a coin toss will be performed. The remaining quadrants will be bonded with alternate composite resin. After bonding, intraoral scans will be performed from baseline to 6 months for every 2 months. Stl files obtained from the scans will be imported to NemoStudio, to evaluate the volume loss of the attachments.

Interventions

Patient's upper right segment will be bonded with GC Aligner Connect. Upper left VOCO, lower left GC, lower right VOCO.

Patient's upper right segment will be bonded with VOCO AlignerFlow LC. Upper left GC, lower left VOCO, lower right GC

Sponsors

Marmara University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
14 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Receiving Invisalign treatment at the Clinic of the Department of Orthodontics, Faculty of Dentistry, Marmara University * Mild to moderate crowding * Exhibiting good oral hygiene * No active dental caries * Voluntarily agreeing to participate in the study and signing the written informed consent form * Having no history of any syndrome, systemic disease, or allergy

Exclusion criteria

* Being pregnant or lactating * Presenting with advanced periodontal disease of a severity that could affect orthodontic treatment * Having prosthetic restorations within the oral cavity * Presenting with white spot lesions prior to orthodontic treatment

Design outcomes

Primary

MeasureTime frameDescription
Within-patient difference between composites in volume wearFrom baseline to 6 monthsAfter importing stl files to NemoStudio software, T0 (without attachments), T1(immediately after bonding) and T4(6 months) scans will be superimposed using surface registration. Using Booleans extractions, T0 model will be removed from T1 and T4, leaving only the attachments. Software will calculate the volumes of attachments in mm³.

Countries

Turkey (Türkiye)

Contacts

STUDY_DIRECTORHanife Nuray Yılmaz

Marmara University Faculty of Dentistry Department of Orthodontics

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 11, 2026