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

Recruiting N/A Interventional Study
Endodontic Treatment
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 – 75
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
63 (estimated)
Sponsor
Lumendo AG · Industry
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About This Trial
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 radiogr…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: • Patients aged 18-75 years with ASA (American Society of Anesthesiologists) classification 1 and 2. ASA 1: A normal healthy patient. Example: Fit, non-obese BMI (Body Mass Index) under 30, a non-smoking patient with good exercise tolerance. ASA 2: A patient with mild systemic…
Contacts

Anupama Tripathi

+4144 589 68 03

anupama.tripathi@odne.co

CONTACT