A Study to Assess the Clinical Success of Root Canal Treatment Using Novel Obturation Material.
Condition(s) studied
Investigational drug(s) / intervention(s)
Endofill: Endofill is intended for the permanent obturation of root canals following root canal preparation and disinfection.
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.
Eligibility
Primary outcome measure(s)
- Effectiveness of root canal treatment using Endofill — 12 months
To measure effectiveness by assessing overall healing, through rate of reduction in apical periodontitis, from baseline up to 12 months post-procedure by measuring periapical radiolucency size.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Medipol University | Istanbul | Turkey (Türkiye) | Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06312085 on ClinicalTrials.gov ↗ ← All trials in Turkey