Oculopharyngeal Muscular Dystrophy (OPMD)

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Review clinical trials related to Oculopharyngeal Muscular Dystrophy (OPMD). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Natural History of Oculo-Pharyngeal Muscular Dystrophy (OPMD) - Israel National OPMD Registry

The goal of this open prospective multi-disciplinary observational study of patients with OPMD at various stages of clinical manifestations is to explore the natural history of the disease in the Israeli population.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Sheba Medical CenterUpdated: Aug 28, 2025Locations: 1Duration: 5 Years
Eligibility criteria

Patients with clinical diagnosis of OPMD or patients with signs /symptoms sugges...

Age <18 years and Pregnancy

Status: Recruiting

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, individuals and researchers to help in the advancement of research in over 7,000 rare diseases. The registry is free for patients to enroll and researchers to access. Visit sanfordresearch.org/CoRDS to enroll.

Participants needed: 20,000
Trial details
Biological sex: AllType: ObservationalSponsor: Sanford HealthUpdated: May 29, 2025Locations: 2Duration: 100 Years
Eligibility criteria

Diagnosis of a rare disease, a disease of unknown prevalence, undiagnosed or an...

Diagnosis of a disease which is not rare