Oral Specimen and Data Acquisition Study of Subjects Requiring Third Molar Removal
Part of paid clinical trials in Bethesda, Maryland.
- Sponsor
- National Institute of Dental and Craniofacial Research (NIDCR)
- Study ID
- NCT01805869
- Status
- Recruiting
Conditions
- Diseases
- Stomatognatic
- Tooth
- Tooth Diseases
- Tooth Impaction
Eligibility Criteria
- Sex
- ALL
- Age
- 16 Years - 50 Years
- Healthy Volunteers
- Accepted
Study Details
Background: \- The third molars (wisdom teeth) normally grow in during late adolescence or early adulthood. Many people need or choose to have these teeth removed with oral surgery. Normally, the removed teeth and tissue are thrown away as medical waste. However, oral health researchers want to collect the teeth and tissue for research. They also want to encourage dentists at the National Institutes of Health to improve their skills in oral surgery. This study will collect the teeth and tissue of people who need to have oral surgery to remove their wisdom teeth. Objectives: * To provide continued dental skills training for dentists at the National Institutes of Health. * To collect teeth and tissue samples following wisdom tooth removal surgery. Eligibility: \- Individuals between 16 and 50 who need to have their wisdom teeth removed. Design: * This study will involve a minimum of three visits. There will be a screening visit, a surgery visit, and at least one follow-up visit. * Participants will be screened with a physical exam and medical history. A full dental exam with x-rays will be given to evaluate the need for surgery. * At the second visit, participants will have oral surgery to remove their wisdom teeth. The teeth and tissue removed during the surgery will be collected for study. * Participants will receive drugs to control the pain after surgery. They will also be able to contact a dentist if there are any problems. * Between 7 and 21 days after surgery, participants will have a followup visit to check the healing. If they are having no problems, this will be the last visit. If there are any postsurgery issues, they will be scheduled for additional visits as needed.
Key Dates
- Start date
- Jun 19, 2013
- Status verified
- Jun 2026
- Primary completion
- Dec 31, 2029
Study Design
- Enrollment
- 10,000 participants (estimated)
Arms
- Arm: Healthy volunteersMale or female ages 16-50
Primary Outcome Measure
data collection [ Time Frame: 16 years ]
Central Contacts
- Sharon Mitchell(301) 496-4372
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| National Institutes of Health Clinical Center | Bethesda | Maryland | 20892 | - |