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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and OthersCharcot-Marie-Tooth disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, central nervous system malformation, hereditary disease, hereditary motor and sensory neuropathy, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathyRecruitingNot stated2025-10-07NCT01193075

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Research sitesCityCountryLinked trials
C. Besta Neurological InstituteMilanItaly1
Cedars-Sinai Medical CenterLos AngelesUnited States392
Children's Hospital of PhiladelphiaPhiladelphiaUnited States434
Children's National HospitalWashington D.C.United States100
Harvard/Massachusetts General HospitalBostonUnited States2
Johns Hopkins UniversityBaltimoreUnited States60
National Hospital of Neurology and NeurosurgeryLondonUnited Kingdom2
Nemours Children's HealthOrlandoUnited States8
Nemours Children's HospitalOrlandoUnited States84
Seattle Children's HospitalSeattleUnited States281
St. Jude Children's Research HospitalMemphisUnited States4
Stanford UniversityPalo AltoUnited States51
The Hospital for Sick ChildrenTorontoCanada20
University Of Colorado HospitalAuroraUnited States106
University of Connecticut/Connecticut Children's Medical CenterHartfordUnited States1
University of IowaIowa CityUnited States284
University of MiamiMiamiUnited States327
University of MichiganAnn ArborUnited States538
University of MinnesotaMinneapolisUnited States325
University of PennsylvaniaPhiladelphiaUnited States507
University of RochesterRochesterUnited States360
University of WestmeadSydneyAustralia1