Actively Recruiting

Age: 18Years +
All Genders
ID07297836

Description of Professional Practices Regarding Treatment of Non-vital Primary Teeth Among Dental Surgeons in France

Led by University Hospital, Strasbourg, France · Updated on 2026-03-03

100

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to describe how dental surgeons in France treat non-vital primary teeth affected by conditions such as irreversible pulpitis, pulp necrosis, and apical periodontitis. It focuses on understanding the current professional practices, including treatment choices, any reservations dentists may have, and the criteria guiding their decisions. The study is observational and seeks to provide data where French information is currently limited. The study involves observing dental surgeons who treat children with affected primary teeth. It considers treatments like pulpectomy, which is recommended by the American Academy of Pediatric Dentistry and requires strict disinfection and use of appropriate materials. Another treatment option considered is lesion sterilization tissue repair (LSTR), which uses topical antibiotics and is somewhat controversial. The study does not involve experimental interventions but gathers information on actual treatment practices. Participants will be dentists treating children, and the study will collect data on their professional practices over up to one year. Researchers will analyze how dentists manage these dental conditions and document the variety of treatment approaches used. The primary outcome is a detailed description of treatment practices by dentists in France. There is no intervention or follow-up beyond this data collection phase, and participation duration aligns with the observation period of up to one year.

CONDITIONS

Brief Title

Professional Practices Regarding Treatment of Non-vital Primary Teeth Among Dental Surgeons in France

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Being a dentist treating children
Not Eligible

You will not qualify if you...

  • Being a dentist treating children

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 (in-person)

Surveillance

Duration - Up to 1 year

Participants who undergo routine care are observed regarding their professional practices in treating non-vital primary teeth.

Periodic observations during routine practice

Trial Site Locations

Total: 1 location

1

Service de Médecine et Chirurgie Bucco-dentaires - CHU de Strasbourg - France

Strasbourg, France, 67091

Actively Recruiting

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Research Team

F

François CLAUSS, DDS, PhD

N

Nhat Minh DO, DDS

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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