Artificial Root-End Barriers

NCT00595842 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2012-03-08

No results posted yet for this study

Summary

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

Conditions

  • Dental Cements
  • Tooth Abnormalities

Sponsors & Collaborators

  • 59th Medical Wing

    collaborator FED
  • The University of Texas Health Science Center at San Antonio

    lead OTHER

Principal Investigators

  • David Holden, DMD · University of Texas

Eligibility

Min Age
5 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-02-28
Primary Completion
2008-06-30
Completion
2008-06-30

Countries

  • United States

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 NCT00595842 on ClinicalTrials.gov