Artificial Root-End Barriers

Completed

• Conditions: Dental Cements; Tooth Abnormalities

• Registration Number: NCT00595842
• Lead Sponsor: The University of Texas Health Science Center at San Antonio

Brief Summary

This study retrospectively looks to determine the clinical success of ProRoot MTA used as an artificial apical barrier in teeth with immature apices.

Detailed Description

The normal development and maturation of a root depends on a vital, healthy pulp. If the pulp becomes necrotic in a tooth with an immature apex, endodontic treatment can be performed using an artificial barrier technique. Mineral trioxide aggregate (MTA) has become the material of choice to accomplish this procedure, however, few studies have evaluated its clinical success. The purpose of this retrospective study was to determine the clinical success of ProRoot MTA used as an artificial apical barrier. Twenty patients were included in this study. After approximately one week of Ca(OH)2 treatment, each patient had MTA placed as an apical barrier in a tooth with a single canal and open apex followed by placement of a final restoration. Patients were recalled and evaluated for clinical signs and symptoms and osseous healing. Immediate post-treatment and recall radiographs were evaluated by two endodontists calibrated for use of the Periapical Index (PAI).

Study Timeline

• Study Start: 2007-02
• Study First Submitted: 2008-01-07
• Study First Submitted QC: 2008-01-15
• Study First Posted: 2008-01-16
• Primary Completion: 2008-06
• Study Completion: 2008-06
• Status Verified: 2012-03
• Last Update Submitted: 2012-03-07
• Last Update Posted: 2012-03-08

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

• a tooth with a single canal and presence of an open apex by radiograph
• Ca(OH)2 treatment for at least one week prior to obturation
• use of MTA to produce an artificial apical barrier
• placement of a final restoration
• radiographs codumenting pretreatment and immedicate post-treatment conditionof the tooth
• patients ages 5-40 years old

Exclusion Criteria

• patients younger than 5 and greater than 40 years old
• patients unable to be contacted for recall during the study
• patients with a medical condition whose health would be jeopardized by participation in the study

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Trial Locations

Locations (1)

University of Texas Health Science Center; 🇺🇸 San Antonio, Texas, United States