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:
2025-12-25 @ 3:13 AM
Ignite Modification Date:
2025-12-25 @ 3:13 AM
NCT ID:
NCT06135805
Eligibility Criteria:
Inclusion Criteria:
* Clinical and histologic diagnosis of Lichen Planus Orale;
* Presence of symptoms related to Lichen Planus Orale;
* Clinical follow-up period of at least 12 weeks;
* Acceptance of informed consent
Exclusion Criteria:
* State of pregnancy or lactation; h
* Histologic signs of dysplasia;
* Medications that induce a lichenoid response (ACE inhibitors, β-blockers, etc.);
* Presence of amalgam fillings in the vicinity of lesions;
* Treatment of oral lichen in the previous 6 months from the start of the program;
* Presence of extraoral lesions (genital, skin, etc.);
* Diabetes being treated with oral hypoglycemic drugs;
* History of previous immunodeficiency;
* HIV seropositivity;
* Previous allogeneic bone marrow transplantation;
* Diagnosis of LES or other autoimmune disease
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
80 Years
Study:
NCT06135805
Study Brief:
Protocol Section:
NCT06135805