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Recruiting NCT01568697

NCT01568697 Oral Bacteria and Immune System Problems Involved in Gum Disease (Periodontitis)

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Clinical Trial Summary
NCT ID NCT01568697
Status Recruiting
Phase
Sponsor National Institute of Dental and Craniofacial Research (NIDCR)
Condition Immunosuppression
Study Type OBSERVATIONAL
Enrollment 700 participants
Start Date 2012-10-05
Primary Completion

Eligibility & Interventions

Sex All sexes
Min Age 7 Years
Max Age 100 Years
Study Type OBSERVATIONAL

Eligibility Fast-Check

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What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 700 participants in total. It began in 2012-10-05.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Background: \- Gum disease is a condition in which the tissue around the tooth root becomes swollen and infected. This condition can cause tooth loss if it is not treated. Who gets gum disease and how bad it will be depends on (1) the different bacteria in the mouth and (2) how the immune system of an individual handles these bacteria. Researchers want to look at the oral bacteria and genetic immune problems of different people to learn how these affect gum disease and other conditions of the mouth. Objectives: \- To study how immune system problems may lead to problems in the mouth, including gum disease. Eligibility: * Children and adults at least 7 years of age who have genetic problems with their immune system. * Healthy adults that have periodontal disease * Health adults that do not have periodontal disease Design: * This study will involve a screening visit and a study visit. * Participants will be screened with a medical history, blood work and a full oral and dental exam, including dental x-rays and photos. * The study visit will involve collection of blood, urine, and other samples, including saliva, plaque, and gum swabs. Any abnormal tissue will sampled for a biopsy. Additional oral and dental exams will be performed. Participants will also answer questions about any current medical or dental problems.

Eligibility Criteria

* INCLUSION CRITERIA: Subjects with Genetic Immune Defects: Patients with a known genetic immune defect will be eligible for screening inclusion under this protocol. * Diagnosed with a genetic immune defect * Willing to allow genetic testing * 7 years old Subjects with Severe Periodontitis of Suspected Genetic Etiology: * History of severe periodontitis prior to age \<30 * Willing to allow genetic testing -\>=7 years old * In good general health Family members of Subjects with Severe Periodontitis of Suspected Genetic Etiology: -Willing to allow genetic testing -\>=7 years old Healthy Volunteer Subjects (with/without periodontitis): * In good general health -\>=18 years old * Willing to allow genetic testing * Have a minimum of 20 natural teeth Inclusion Criteria for Natural History phase, all subjects: * Diagnosis of genetic immune defect * Presence of oral manifestation (primarily periodontitis) Criteria for standard of care treatment: * Active untreated disease (visible signs of tissue inflammation including erythema/edema, generalized bleeding upon probing) * Periodontal disease defined as bone loss of \>=5mm as measured on periodontal exam. EXCLUSION CRITERIA: All Subjects: * History of Hepatitis B or C * History of HIV * Prior radiation therapy to the head or neck * Have an active malignancy except localized basal or squamous cell carcinoma of the skin * Have been treated with systemic chemotherapeutics or radiation therapy within 5 years of screening * Pregnant or lactating * If participation in the protocol would not be safe or in the subject s best interest in the opinion of either the PI or the primary medical team. Additional Exclusions for Healthy Volunteers: * Diagnosis of diabetes and/or HbA1C level \>6% * More than 3 hospitalizations in the last 3years * Have an autoimmune disorder such as Lupus, Rheumatoid arthritis, etc. * In the 3 months before study enrollment, have used any of the following: * Systemic (intravenous, intramuscular, or oral) antibiotics * Oral, intravenous, intramuscular, intranasal, or inhaled corticosteroids or other immunosuppressants (e.g., cyclosporine) * Cytokine therapy * Methotrexate or immunosuppressive chemotherapeutic agents * Large doses of commercial probiotics (\>=10\^8 colony-forming units or organisms per day); includes tablets, capsules, lozenges, chewing gum, or powders in which a probiotic is a primary component; ordinary dietary components such as fermented beverages/milks, yogurts, and foods do not apply * Have used tobacco products (including e-cigarettes) within 1 year of screening * Unwillingness to consent to oral biopsy * NIH employees working in the Oral Immunity and Inflammation Unit and members of the Clinical Research Core Team will not be eligible for enrollment. Additional Exclusions for Standard of Care Treatment at NIH: * Mild/moderate non-active disease (absence of active inflammatory lesions) * Subjects with urgent/complex restorative needs (ex. severe active carious lesions/fractured dentition) * Subjects in need for advanced prosthetic needs (including implants and restorations)

Contact & Investigator

Central Contact

Laurie D Brenchley, R.D.H.

✉ laurie.brenchley@nih.gov

📞 (301) 451-2551

Principal Investigator

Niki M Moutsopoulos, D.D.S.

PRINCIPAL INVESTIGATOR

National Institute of Dental and Craniofacial Research (NIDCR)

Frequently Asked Questions

Who can join the NCT01568697 clinical trial?

This trial is open to participants of all sexes, aged 7 Years or older, up to 100 Years, studying Immunosuppression. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT01568697 currently recruiting?

Yes, NCT01568697 is actively recruiting participants. Contact the research team at laurie.brenchley@nih.gov for enrollment information.

Where is the NCT01568697 trial being conducted?

This trial is being conducted at Bethesda, United States.

Who is sponsoring the NCT01568697 clinical trial?

NCT01568697 is sponsored by National Institute of Dental and Craniofacial Research (NIDCR). The principal investigator is Niki M Moutsopoulos, D.D.S. at National Institute of Dental and Craniofacial Research (NIDCR). The trial plans to enroll 700 participants.

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