Meibomian Gland Probing for Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis
Trial Summary
What is the purpose of this trial?
The investigators' aim is to study the effects of mechanical expression of meibomian glands on eyelid disease, ocular surface health in the subacute phase of SJS/TEN. The primary outcome is to use meibomian gland imaging to assess the health and caliber of the meibomian glands of both lower eyelids, between the treated and non-treated eyes before and after the intervention. Monitoring of outcomes will be measured by comparing the results of meibography at the initial visit and at the 6-month follow-up. The secondary outcome assessed will be patient symptoms. The Ocular Surface Disease Index survey will be administered before each treatment and patients will be asked to differentiate their symptoms between the two eyes, both before and after the intervention. The investigators hypothesize that mechanical expression of meibomian glands within the first 6 months of SJS/TEN onset will significantly improve ocular surface disease and symptoms in those patients.
Research Team
Eligibility Criteria
Adults over 18 with Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis (SJS/TEN) who are in the sub-acute phase (within 6 months of onset) and have meibomitis can participate. Those under 18, past the sub-acute phase, without meibomitis, or with unconfirmed SJS vs. other conditions cannot join.Inclusion Criteria
Exclusion Criteria
Treatment Details
Interventions
- Meibomian Gland Probing (Other)
Find a Clinic Near You
Who Is Running the Clinical Trial?
Massachusetts Eye and Ear Infirmary
Lead Sponsor
CarolAnn Williams
Massachusetts Eye and Ear Infirmary
Chief Executive Officer
MBA from Harvard Business School
Aalok Agarwala
Massachusetts Eye and Ear Infirmary
Chief Medical Officer since 2019
MD from University of California, Los Angeles