CompletedNot Applicable

Effectiveness of Methods to Remove Residual Orthodontic Adhevsie

Iraq40 participantsStarted 2023-05-01

Plain-language summary

The aim of this study is to compare the clinical efficacy of different residual orthodontic adhesive removing methods for rebonding debonded metal attachments.

Who can participate

Age range12 Years – 25 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. Patients need metal fixed orthodontic appliance treatment;
✓. Complete set of permanent dentition with fully erupted teeth on both arches;
✓. Intact teeth and mainly their buccal surfaces are free from caries, fillings, or gingival hyperplasia;
✓. No occlusal interferences that can affect the ideal position of attachments, especially in the lower arch.

Exclusion criteria

✕. patients have crown, missing teeth, or craniofacial anomalies.
✕. patients have congenital enamel defects specially their buccal surface.

What they're measuring

The number of bonding failures will be compared using the chi-square test.

Timeframe: baselines

Trial details

NCT IDNCT05929391

SponsorUniversity of Baghdad

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-02-01

View on ClinicalTrials.gov More Orthodontic Appliance Complication trials