Ignite Creation Date:
2024-05-05 @ 10:17 AM
Last Modification Date:
2024-10-26 @ 9:02 AM
Study NCT ID:
NCT00001600
Status:
COMPLETED
Last Update Posted:
2008-03-04
First Post:
1999-11-03
Brief Title:
Diagnosis and Evaluation of Patients Needing Third Molar Wisdom Tooth Extraction and Patients With Chronic Facial Pain
Sponsor:
National Institute of Dental and Craniofacial Research NIDCR
Organization:
National Institutes of Health Clinical Center CC
Study Overview
Official Title:
Diagnosis and Evaluation of Patients in Need of Third Molar Removal or Suffering From Chronic Facial Pain
Status:
COMPLETED
Status Verified Date:
2005-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
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
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
Detailed Description:
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 subjects 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 physiciandentist
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 subjects 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 physiciandentist
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 97-D-0163 | None | None | None |