MedTrace Logo

Safety and Efficacy of the Apexum Ablator

NCT00762840 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2009-06-05

No results posted yet for this study

Summary

The study is designed to test the hypothesis that there is a difference in healing kinetics and healing rate between teeth treated by conventional endodontic procedure alone and those in which such procedure was supplemented with the Apexum Ablator protocol

Conditions

  • Periapical Periodontitis

Interventions

DEVICE

the Apexum Protocol

using the apexum kit for minimally invasive removal of periapical lesion tissue.

PROCEDURE

Conventional endodontic procedure

Standard root canal treatment

Sponsors & Collaborators

  • Monitoring: Quail CRO, Romania

    collaborator UNKNOWN

  • Medistat Ltd., Israel

    collaborator INDUSTRY

  • Apexum Ltd.

    lead INDUSTRY

Principal Investigators

  • Dragos Slavescu, DMD · Titu Maiorescu University

  • Dan Dragomirescu, DMD · Cabinet Stomatologic Dr Dan Dragomirescu

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-10-31
Primary Completion
2010-04-30

Countries

  • Romania

Study Locations

More Related Trials

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 NCT00762840 on ClinicalTrials.gov