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Post-Debonding Finishing in Orthodontics

Post-Debonding Finishing: Analysis of Clinical Approaches for Maintaining Enamel Health

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07534423
Enrollment
100
Registered
2026-04-16
Start date
2024-01-01
Completion date
2026-06-01
Last updated
2026-04-20

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

Conditions

Caries, Enamel Lesions

Keywords

Orthodontic, Enamel integrity, debonding

Brief summary

This study investigates clinical approaches to orthodontic debonding and post-debonding finishing, focusing on enamel preservation. An observational epidemiological survey was conducted among dental professionals to assess commonly used techniques, instruments, and complications. Results highlight variability in clinical protocols, with mechanical methods being the most widely adopted. The study emphasizes the importance of minimally invasive strategies to reduce enamel damage and improve patient outcomes.

Detailed description

This study explores orthodontic debonding and post-debonding finishing procedures, with particular emphasis on their impact on enamel integrity and long-term oral health. The study is an observational epidemiological investigation aimed at identifying current clinical practices, materials, and associated complications. The research was conducted using an online questionnaire developed using Google Forms. The survey consisted of 23 questions (19 multiple-choice and 4 open-ended) and was distributed to dental professionals involved in orthodontic practice. Participants included orthodontists, general dentists with orthodontic experience, and orthodontic residents. The questionnaire was structured into four sections: demographic and professional data, instruments and techniques used for debonding and polishing, clinical complications observed, and post-treatment management strategies. Inclusion criteria required professional involvement in orthodontic procedures and informed consent, while non-relevant dental professionals were excluded. Data were anonymized and analyzed using spreadsheet software.

Interventions

None listed

Sponsors

University of Roma La Sapienza
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Professional Background: Must be a dental professional with specific clinical knowledge and practical skills required to perform orthodontic therapies. * Specialization: Eligible participants must fall into one of the following categories: Orthodontist (Specialist), General Dentist with demonstrated clinical competence in orthodontics, Resident/Post-graduate student specializing in Orthodontics and Dentofacial Orthopedics.

Exclusion criteria

* Non-Orthodontic Professionals: Dental professionals who do not belong to the categories mentioned above are excluded, even if they work within the dental field. * Lack of Specific Competence: Practitioners who do not possess the necessary clinical expertise to perform orthodontic debonding and finishing procedures. * Incomplete Participation: Failure to provide informed consent or complete the mandatory sections of the epidemiological survey.

Design outcomes

Primary

MeasureTime frameDescription
Prevalence and Type of Iatrogenic Enamel Damage Post-Orthodontic DebondingAt the completion of the orthodontic treatment (immediate post-debonding phase).Evaluation of the frequency and nature of enamel alterations (e.g., fractures, scratches, or surface roughness) observed by practitioners following the removal of orthodontic brackets and residual resin. This measure assesses the clinical impact of different debonding and finishing protocols on enamel integrity. Higher scores indicate a worse outcome (higher frequency of iatrogenic damage)
Frequency of Patient-Reported Dental Sensitivity and PainFrom the start of the debonding procedure up to the first follow-up visit (typically within a few weeks).Assessment of the incidence of hypersensitivity (to thermal or tactile stimuli) and discomfort/pain reported by patients during or immediately after the debonding and finishing procedures.

Countries

Italy

Contacts

CONTACTFabrizio Guerra
fabrizio.guerra@uniroma1.it3283150627

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 21, 2026