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 @ 2:53 AM
Ignite Modification Date:
2025-12-25 @ 2:53 AM
NCT ID:
NCT04914533
Eligibility Criteria:
Inclusion Criteria:
* Demonstrates understanding of the study and willingness to participate as evidenced by voluntary written informed consent and has received a signed and dated copy of the informed consent form.
* 18 years and older.
* Self report canker sore outbreaks once every 30 days or more frequent
* Understands and is willing, able and likely to comply with all study procedures and restrictions.
* No previous experience of LLLT.
* United States resident.
* Willingness and ability to submit a $49 deposit using a credit card for the device.
Exclusion Criteria:
* Patients with a known systemic disease that predisposes them to RAS (e.g., Behçet disease) or undergoing systemic treatment for RAS.
* The presence of a serious medical condition.
* Currently known to be pregnant or breastfeeding
* Patients treated with topical or systemic medication for RAS, such as corticosteroid therapy, antibiotics or analgesics during the previous month.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT04914533
Study Brief:
Protocol Section:
NCT04914533