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Oculopharyngeal Muscular Dystrophy (OPMD)

Clinical trial condition

Oculopharyngeal Muscular Dystrophy (OPMD)

Explore clinical trials studying Oculopharyngeal Muscular Dystrophy (OPMD). Study availability and eligibility vary by location and protocol.

2 public trials 2 recruiting studies

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Oculopharyngeal Muscular Dystrophy (OPMD) trial results

Recruiting

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

NCT07146256

Conditions: Blepharoptosis, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Deglutition Disorders, +22 more
Locations: Sheba Medical Center Ramat Gan, Israel

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Recruiting

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

NCT01793168

Conditions: 1p36 Deletion Syndrome, 3-Methylglutaconic Aciduria, Type V, 4p Deletion Syndrome, Non-Wolf-Hirschhorn Syndrome, +698 more
Locations: Sanford Health Sioux Falls, South Dakota, United States

Online Patient Enrollment System Sydney, Australia

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