Stevens Johnson Syndrome

4

Review clinical trials related to Stevens Johnson Syndrome. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Subconjunctival Humira for Boston Keratoprosthesis

This trial is studying the safety and tolerability of receiving an injection of adalimumab (Humira) during the Boston Keratoprosthesis (KPro) surgery.

Participants needed: 8
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Massachusetts Eye and Ear InfirmaryUpdated: Mar 27, 2026Locations: 1
Eligibility criteria

Age 18 years or older [+6]

Active tuberculosis or untreated latent tuberculosis (e.g., positive interferon-... [+18]

Status: Not yet recruiting

Autologous Serum Obtained by a Closed-Circuit Collection Device

Autologous serum eye drops (ASED) are an established therapy for ocular surface diseases; however, their preparation can be costly and may not be available due to the need for germ-free conditions. This pilot trial assesses the feasibility of collecting ASED in a closed-circuit system for patients with chronic ocular surface diseases.

Participants needed: 16
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: GIANCARLO FATOBENEUpdated: Jun 10, 2025Locations: 1
Eligibility criteria

≥ 18 years [+2]

Active ocular infection; [+9]

Status: Recruiting

Drug Reactions Sampling (COLLECTIONTOXIDERMIES)

Intro: Dermatology department of Henri Mondor Hospital (Creteil, France), is a reference center for toxic bullous diseases and severe cutaneous drug reactions (Stevens-Johnson syndrome (SJS), Lyell syndrome (toxic epidermal necrolysis (TEN)), generalized bullous fixed drug reactions, AGEP, DRESS, drug induced immunoglobulin A (IgA) bullous dermatosis, and erythema multiforme). In order to conduct clinical and biological research studies in drug reactions, it is necessary for the investigator's department to implement a collection of clinical data and biological samples. Hypothesis/Objective: To collect clinical data and cutaneous and biological samples for immunological, biological and genetic studies to improve knowledge about pathophysiology of drug reactions. Method: The following samples will be performed in addition to the routine practice samples: one skin punch biopsy (6mm); 43 mL of blood; blister fluid aspiration; oral and nose mucous membrane and skin eSWABs, stool samples. These samples will be stored in a dedicated biological sampling department ("Platform of biological resources"). Conclusion: The implementation of this collection should allow us to conduct pathophysiological studies about drug reactions.

Participants needed: 500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Assistance Publique - Hôpitaux de ParisUpdated: May 3, 2022Locations: 1
Eligibility criteria

Patient ≥ 18 y-old [+3]

Patients law protection

Status: Available

Clinical Trial on the Effect of Autologous Oral Mucosal Epithelial Sheet Transplantation

To investigate the effect of ocular surface reconstruction and assess the safety in cultivated oral mucosal epithelial cell sheet transplantation (COMET) regarding patients with cicatricial change of ocular surface.

Trial details
Age: 16+Biological sex: AllType: Expanded AccessSponsor: Seoul National University HospitalUpdated: Apr 20, 2016Locations: 2
Eligibility criteria

patient with eye which has limbal stem cell deficiency and conjunctivalization o... [+4]

patient who has relevant corneal transparency [+6]