Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07019298

Success of Endodontic Treatment With Different Obturation Techniques and Sealer Cements

Led by University of Siena · Updated on 2025-06-13

270

Participants Needed

1

Research Sites

208 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The present study aims to compare the radiographic success of endodontic treatment using Orstavik's criteria between two sealers: AH Plus (Dentsply DeTrey, Konstanz, Germany) and Neosealer Flo (Avalon Biomed, Bradenton, Florida, USA), as well as between two obturation techniques: continuous wave and single cone. The study includes 270 patients, with a minimum follow-up period of 6 months. Clinical and radiographic variables will be assessed, including quality of obturation, lesion healing, and restoration. The study seeks to determine if the use of bioceramic sealer is effective regardless of the obturation technique used, highlighting the importance of clinical follow-up to evaluate endodontic treatment success.

CONDITIONS

Official Title

Success of Endodontic Treatment With Different Obturation Techniques and Sealer Cements

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years and older
  • Teeth diagnosed with pulpal necrosis or irreversible pulpitis
  • Provided informed consent for data usage
Not Eligible

You will not qualify if you...

  • Patients with systemic conditions that may impair healing, such as uncontrolled diabetes or immunosuppression
  • Teeth with root fractures, resorption, or open apices
  • Incomplete clinical or radiographic records
  • Poor-quality radiographs or lack of standardization for evaluation

AI-Screening

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Trial Site Locations

Total: 1 location

1

Universidad Rey Juan Carlos

Madrid, Spain, Spain, 28922

Actively Recruiting

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Research Team

G

Giulia Malvicini, DDS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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