RETT Syndrome With Proven MECP2 Mutation

Explore clinical trials studying RETT Syndrome With Proven MECP2 Mutation. Study availability and eligibility vary by location and protocol.

5 public trials 2 recruiting studies

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RETT Syndrome With Proven MECP2 Mutation trial results

Recruiting

NCT07493096

Conditions: 22q11 Deletion Syndrome, 22q11.2 Deletion Syndrome, Abnormalities, Multiple, +81 more
Locations: Ability and Beyond The Woodlands, Texas, United States

Recruiting

NCT07430046

Conditions: Cognition Disorders, Cognitive Dysfunction, Mental Disorders, +7 more
Locations: Unità di Neuropsichiatria Infantile, IRCCS, Istituto Giannina Gaslini, Genova Genova, Italy

UOC di Neuropsichiatria Infantile, Policlinico Universitario "Gaetano Martino" di Messina, University of Messina. Messina Messina, Italy

Centro Epilessia - Unità Neurologia Pediatrica, ASST Ospedale Santi Carlo Paolo - Dipartimento Scienze della Salute, Università di Milano Milan, Italy

Unità di Pediatria, Dipartimento della Donna e dei Bambini - Policlinico S. M. alle Scotte. Siena Siena, Italy

Enrolling by Invitation

NCT06739434

Conditions: RETT Syndrome With Proven MECP2 Mutation
Locations: Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Shanghai, Shanghai Municipality, China

Not Yet Recruiting

NCT07257978

Conditions: Chemically-Induced Disorders, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +12 more
Locations: Monash Health Clayton, Victoria, Australia

Completed

NCT02110797

Conditions: Bone Diseases, Bone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +14 more
Locations: Kremlin bicêtre Bicêtre, France