retinal dystrophy, optic nerve edema, splenomegaly, anhidrosis, and migraine headache syndrome | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Familial Mediterranean Fever and Related Disorders: Genetics and Disease Characteristics	Body Temperature Changes, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Fever, Headache, Hypertrophy, Hypohidrosis, Neurologic Manifestations, Pain, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Skin and Connective Tissue Diseases, Splenomegaly, eye disorder, familial Mediterranean fever, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinal dystrophy, optic nerve edema, splenomegaly, anhidrosis, and migraine headache syndrome, skin disorder, sweat gland disorder	Recruiting	Not stated	2026-10-08		NCT00001373
A Method Characterization Study to Evaluate Thermoregulatory Sweat Production in Healthy Volunteers and Patients With ROSAH Syndrome)	Hypohidrosis, Skin and Connective Tissue Diseases, anhidrosis, retinal dystrophy, optic nerve edema, splenomegaly, anhidrosis, and migraine headache syndrome, skin disorder, sweat gland disorder	Not yet recruiting	Not applicable	2026-09-10		NCT07814209
Evaluating the Safety and Tolerability of Orally Administered DF-003 in ROSAH Syndrome Patients	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, cone-rod dystrophy, eye disorder, hereditary disease, inherited retinal dystrophy, macular degeneration, macular retinal edema, retinal degeneration, retinal disorder, retinal dystrophy, optic nerve edema, splenomegaly, anhidrosis, and migraine headache syndrome, uveal disorder, uveitis	Recruiting	Phase 1	2026-06-05		NCT06395285