Facial Pain Clinical Trial
Official title:
Diagnosis and Evaluation of Patients in Need of Third Molar Removal or Suffering From Chronic Facial Pain
This study provides a mechanism for evaluating patients for possible participation in NIDCR
clinical research studies. NIDCR studies involve three major areas-pain, neurosensory
mechanisms, and pain-relieving drugs-all of which have specific requirements and patient
characteristics. No treatment is offered under this protocol; it is intended to facilitate
patient recruitment into NIDCR studies.
Patients with unusual or unknown conditions that have or have not been diagnosed may be
eligible for this screening study. Specific medical criteria for enrollment vary with the
particular protocol for which the individual is being screened. Medical and dental histories
will be obtained and participants will have a dental examination. Diagnostic procedures will
be done in accord with standard medical and dental practice and may include X-rays, blood
tests, and routine urinalysis, as appropriate. Participants found eligible for an active
study may enroll in that study. Those who are not eligible for a current study may be
re-evaluated for future studies within a year if they wish. After 1 year, participants for
whom no appropriate studies are identified will be referred back to their primary doctor or
referring physician or dentist.
This protocol is designed to screen individuals with either third molars ("wisdom teeth") in
need of removal, or with chronic orofacial pain as potential research subjects.
Each individual will be thoroughly evaluated during the screening process, including past
medical history and an appropriate physical examination. Other routine diagnostic procedures
and tests may also be completed in order to help determine a subject's eligibility. These
tests and procedures are of minimal risks and will be described in more detail in section
III: "Study Procedures".
Once the screening process is completed and eligibility determined, the subjects will be
informed of their options to participate in one or more of the current NIDCR research
studies. If no appropriate protocol is identified, recommendations for other treatment
options may be given to the individual, their primary doctor, or referring
physician/dentist.
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N/A
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