Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:32 PM
Ignite Modification Date:
2025-12-24 @ 7:32 PM
NCT ID:
NCT01808703
Eligibility Criteria:
Inclusion Criteria:
* Adult males or females 18 years or older
* Able and willing to follow study procedures and instructions
* Must have read, understood and signed an informed consent form
* Present with at least 12 teeth in the functional dentition, excluding third molars
* Generalized, moderate to severe chronic periodontitis
* Present with at least two periodontal pockets (on separate teeth) measuring 6 mm or more and that bleed on probing
Exclusion Criteria:
* Gross oral pathology
* Chronic treatment (i.e., two weeks or more) with anti-inflammatory medications (steroids or nonsteroidal anti-inflammatory drugs) or any other medications known to affect periodontal status (e.g., phenytoin, calcium antagonists, cyclosporine and coumadin) within one month of the screening examination
* Antibiotic treatment within 3 month prior to the screening examination
* History of rheumatic fever, valvular disease, valve replacement or prosthetic joint replacement necessitating antibiotic prophylaxis
* Active infectious diseases such as hepatitis, human immunodeficiency virus (HIV) or tuberculosis
* Reported allergies to herbal products
* Taking herbal product supplements
* Severe unrestored caries or any condition that is likely to require antibiotic treatment over the study
* Periodontal therapy (quadrant or maintenance scaling and root planing and/or periodontal surgical therapy) within 6 months prior to enrollment.
* Female patients who report being pregnant or lactating, or female patients who are of childbearing potential and who are not using hormonal, barrier methods of birth control (e.g., oral or parenteral contraceptives, diaphragm plus spermicide, condoms), or abstinence
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01808703
Study Brief:
Protocol Section:
NCT01808703