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Recruiting NCT07692880

NCT07692880 Digital vs. Conventional Indirect Bonding.

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Clinical Trial Summary
NCT ID NCT07692880
Status Recruiting
Phase
Sponsor Azienda Ospedaliero-Universitaria Careggi
Condition Malocclusion
Study Type INTERVENTIONAL
Enrollment 20 participants
Start Date 2025-09-03
Primary Completion 2026-07-20

Eligibility & Interventions

Sex All sexes
Min Age 12 Years
Max Age 18 Years
Study Type INTERVENTIONAL
Interventions
digital indirect bonding techniqueconventional indirect bonding technique

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 20 participants in total. It began in 2025-09-03 with a primary completion date of 2026-07-20.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This randomized split-mouth clinical trial will compare digital and conventional indirect bonding techniques for fixed orthodontic bracket placement in adolescent patients requiring treatment in both dental arches. Each participant will receive both bonding techniques, with allocation of the digital and conventional indirect bonding procedures to the upper or lower arch determined by randomization. The study will evaluate the time required to complete bracket bonding procedures and the early clinical performance of the two techniques, assessed by bracket failure within the first month after appliance placement.

Eligibility Criteria

Inclusion Criteria: * Patients aged 12 to 18 years requiring fixed orthodontic treatment on both upper and lower arches * Presence of full permanent dentition, including erupted second molars Exclusion Criteria: * Presence of dental anomalies in number (supernumerary or missing teeth) in either arch * Orthodontic treatment plans involving tooth extractions in either arch * Nickel allergy * History of cleft lip and/or palate * Craniofacial syndromes

Contact & Investigator

Central Contact

Lorenzo Franchi

✉ lorenzo.franchi@unifi.it

📞 +390557945602

Frequently Asked Questions

Who can join the NCT07692880 clinical trial?

This trial is open to participants of all sexes, aged 12 Years or older, up to 18 Years, studying Malocclusion. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07692880 currently recruiting?

Yes, NCT07692880 is actively recruiting participants. Contact the research team at lorenzo.franchi@unifi.it for enrollment information.

Where is the NCT07692880 trial being conducted?

This trial is being conducted at Florence, Italy.

Who is sponsoring the NCT07692880 clinical trial?

NCT07692880 is sponsored by Azienda Ospedaliero-Universitaria Careggi. The trial plans to enroll 20 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology