Pemphigoid, Benign Mucous Membrane
Pemphigoid, Benign Mucous Membrane
Explore linked clinical trials. Standard reference: MESH:M00161104 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Subconjunctival Humira for Boston Keratoprosthesis | Chemically-Induced Disorders, Conjunctival Diseases, Drug Eruptions, Drug-Related Side Effects and Adverse Reactions, Erythema, Hypersensitivity, Delayed, Pemphigoid, Benign Mucous Membrane, Skin and Connective Tissue Diseases, Stevens-Johnson syndrome, Stomatognathic Diseases, dermatitis, drug allergy, erythema multiforme, eye disorder, immune system disorder, mouth disorder, ocular cicatricial pemphigoid, skin disorder, stomatitis, vesiculobullous skin disease | Not yet recruiting | Phase 1 | 2026-08-31 | NCT06926478 | |
| Proteomic and Metabolomic Lacrimal Fingerprint in Diverse Pathologies of the Ocular Surface | Bacterial Infections and Mycoses, Conjunctival Diseases, Conjunctivitis, Allergic, Eye Infections, Bacterial, Hypersensitivity, Immediate, Infections, Pemphigoid, Benign Mucous Membrane, Skin and Connective Tissue Diseases, bacterial infectious disease, conjunctivitis, corneal disorder, dry eye syndrome, eye disorder, eye infectious disorder, immune system disorder, keratitis, keratoconjunctivitis, keratoconjunctivitis, infectious, lacrimal apparatus disorder, mucous membrane pemphigoid, non-human animal disease, skin disorder, vesiculobullous skin disease | Recruiting | Not stated | 2026-04-27 | NCT04198740 | |
| FARD (RaDiCo Cohort) (RaDiCo-FARD) | Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Conjunctival Diseases, Eye Diseases, Hereditary, Infant, Newborn, Diseases, Keratoderma, Palmoplantar, Neoplasms by Histologic Type, Neoplasms, Nerve Tissue, Nutritional and Metabolic Diseases, Pemphigoid, Benign Mucous Membrane, Skin Abnormalities, Skin and Connective Tissue Diseases, albinism, autoimmune disease, ectodermal dysplasia syndrome, eye disorder, hereditary disease, hereditary neoplastic syndrome, hereditary skin disorder, hypopigmentation of the skin, ichthyosis, immune system disorder, inborn disorder of amino acid metabolism, inborn errors of metabolism, incontinentia pigmenti, inherited epidermolysis bullosa, inherited neurodegenerative disorder, keratosis, metabolic disease, mucous membrane pemphigoid, neoplasm, nerve sheath neoplasm, nervous system disorder, neurocutaneous syndrome, neurodegenerative disease, neurofibroma, neurofibromatosis, neurofibromatosis type 1, neuromuscular disease, pemphigus, peripheral nervous system disorder, skin disorder, skin pigmentation disorder, vesiculobullous skin disease | Recruiting | Not stated | 2026-02-12 | NCT05954416 | |
| Peridontal and Intestinal Microbiota in Patients With Gingival Scarring Pemphigoid | Conjunctival Diseases, Pemphigoid, Benign Mucous Membrane, Skin and Connective Tissue Diseases, eye disorder, skin disorder, vesiculobullous skin disease | Recruiting | Not stated | 2025-03-20 | NCT06291350 |