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A Study to Assess the Clinical Success of Root Canal Treatment Using Novel Obturation Material.

NCT06312085 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 63

Last updated 2024-07-12

No results posted yet for this study

Summary

The goal of this study is prospective, single-arm, non-randomized controlled trial to test the effectiveness, safety and performance of a novel dental obturation material. The main question sit answers is

1. To test the effectiveness of the Endofill device for root canal obturation up to 12-month follow-up period.
2. To test the performance of the Endofill device evaluated with periapical radiographs immediately on completion of procedure.

The participants requiring root canal treatment will be treated with obturated using Endofill material and post-treatment follow-up vistis will be conducted for 1 year. This is a single-arm study with no comparison groups.

Conditions

  • Endodontic Treatment

Interventions

DEVICE

Endofill

Endofill is intended for the permanent obturation of root canals following root canal preparation and disinfection.

Sponsors & Collaborators

  • Avania

    collaborator INDUSTRY

  • Lumendo AG

    lead INDUSTRY

Principal Investigators

  • Tan Firat Eyuboglu, Prof. Dr. · Medipol University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-06-07
Primary Completion
2025-12-31
Completion
2026-12-31

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06312085 on ClinicalTrials.gov