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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00001182
Other study ID # 820057
Secondary ID 82-D-0057
Status Completed
Phase N/A
First received November 3, 1999
Last updated March 3, 2008
Start date April 1982
Est. completion date June 2002

Study information

Verified date June 2002
Source National Institutes of Health Clinical Center (CC)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

This study offers evaluation and treatment of patients with unusual diagnostic or treatment considerations. It is not designed to test new treatments; rather, patients will receive current standard of care treatments. The purposes of the study are: 1) to allow NIDCR staff an opportunity to maintain and improve their clinical skills; and 2) to evaluate referred patients for research potential. (Participants in this protocol will not be required to join a research study; the decision will be voluntary.)

Patients in need of dental/oral diagnosis and therapy of interest to NIDCR staff dentists may be eligible for this protocol. Participants will have a comprehensive dental examination and may receive part or all of their treatment at the NIDCR clinic. Diagnostic procedures, materials and treatments used in this study are limited to those widely accepted in dentistry and are non-experimental in nature.


Description:

The proposed pilot project will allow the staff of the Dental Clinic Oral Medicine Fellowship Program to accept patients, for diagnosis and conventional therapy, which do not otherwise meet the criteria for any of the current NIDCR research protocols. This clinical examination and therapy by Dental Clinic practitioners will provide an excellent forum for the observation of oral conditions and phenomena that may generate scientific inquiries and provide valuable educational experiences consistent with the goals of the Oral Medicine Program.


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date June 2002
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Patients in need of dental/oral diagnosis and therapy which are of interest to one or more of the staff dentists.

Study Design

N/A


Related Conditions & MeSH terms


Intervention

Procedure:
current standard of care treatments


Locations

Country Name City State
United States National Institute of Dental And Craniofacial Research (NIDCR) Bethesda Maryland

Sponsors (1)

Lead Sponsor Collaborator
National Institute of Dental and Craniofacial Research (NIDCR)

Country where clinical trial is conducted

United States, 

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