Actively Recruiting

All Genders
Healthy Volunteers
ID07534423

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

Led by University of Roma La Sapienza · Updated on 2026-04-20

100

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to explore clinical approaches used during orthodontic debonding and the finishing steps after bracket removal, focusing on preserving enamel health and minimizing damage. The study is an observational epidemiological survey conducted among dental professionals including orthodontists, general dentists experienced in orthodontics, and orthodontic residents. It highlights the variability in clinical protocols and emphasizes minimally invasive methods to improve patient outcomes. Dentists involved in orthodontic care were surveyed using a 23-question online questionnaire distributed via Google Forms. The survey covered their professional background, the instruments and techniques they use for debonding and polishing, observed clinical complications, and strategies for post-treatment management. Data were collected anonymously and analyzed to assess common practices and complications associated with post-debonding procedures. Participants are dental professionals who completed the questionnaire, providing demographic and clinical practice information. The study measures include the prevalence and types of enamel damage immediately after orthodontic debonding and the frequency of patient-reported sensitivity and pain from the start of debonding until the first follow-up visit. No specific treatment or intervention is administered, as this is an observational study. The findings aim to inform best practices to protect enamel health during orthodontic care.

CONDITIONS

Brief Title

Post-Debonding Finishing in Orthodontics

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Must be a dental professional with clinical knowledge and skills in orthodontic therapies
  • Must be an Orthodontist, General Dentist with demonstrated orthodontic competence, or Orthodontic Resident/Post-graduate student
  • Must provide informed consent and complete the epidemiological survey
Not Eligible

You will not qualify if you...

  • Dental professionals not in the specified orthodontic-related categories
  • Practitioners lacking the clinical expertise to perform orthodontic debonding and finishing
  • Failure to provide informed consent or complete mandatory survey sections

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (online questionnaire)

Observational Survey Completion

Duration - Single session

Participants complete an online questionnaire about their clinical practices, materials used, and observed complications related to orthodontic debonding and post-debonding finishing.

1 visit (online questionnaire)

Data Analysis and Follow-up

Duration - Up to study completion

Data collected from participants are analyzed to assess enamel damage prevalence and patient-reported outcomes after orthodontic debonding.

No participant visits; observational data only

Trial Site Locations

Total: 1 location

1

Sapienza università di Roma

Roma, RM, Italy, 00161

Actively Recruiting

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Research Team

F

Fabrizio Guerra

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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Published Research Related To This Trial

Effect of orthodontic debonding and adhesive removal on the enamel - current knowledge and future perspectives - a systematic review.

Joanna Janiszewska-Olszowska, Tomasz Szatkiewicz, Robert Tomkowski...

https://pubmed.ncbi.nlm.nih.gov/25327612