Evaluation of Effectiveness and Safety of Intense Pulsed Light Treatment for Chalazion (NCT07405138) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Evaluation of Effectiveness and Safety of Intense Pulsed Light Treatment for Chalazion
United States40 participantsStarted 2026-02-04
Plain-language summary
To study the effectiveness and safety of IPL treatment for Chalazion
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Subject is able to read, understand, and sign an Informed Consent Form (ICF)
* 18 years of age or older
* Clinical diagnosis of chalazion in the inflammatory stage
* Subject is willing to comply with all study procedures-
Exclusion Criteria:
* Concurrent eyelid infection
* Chalazion with atypical features, which to the opinion of the study investigator is inadequate for a study
* Recurring Chalazion
* Floppy eyelid syndrome
* Demodex blepharitis patients taking Lotilaner ophthalmic solution within 30 days prior to screening
* Ocular surgery within 3 months prior to screening
* Current diagnosis of malignant tumors in the affected eyelid, including:
sebaceous carcinoma and basal cell carcinoma
* Laser Assisted In Situ Keratomileusis (LASIK)/Small Incision Lenticule Extraction (SMILE) surgery, within 1 year prior to screening
* Radial Keratotomy (RK) surgery
* Recent ocular trauma, within 3 months prior to screening
* Pre-cancerous lesions or skin cancer in the planned treatment area
* Severe active allergies, or other severe uncontrolled eye disorders affecting the ocular surface
* Uncontrolled infections or uncontrolled immunosuppressive diseases
* Best corrected visual acuity worse than 20/200 in either eye
* Ocular surface abnormality that may compromise corneal integrity in either eye (e.g., prior chemical burn, Epithelial Basement Membrane Dystrophy - EBMD)
* Within 1 week prior to screening, use of photosensitive medication and/or herbs that ma…
What they're measuring
1
The percentage of resolved chalazion 4 weeks after the last treatment in the study group and the control group