RecruitingNCT01193088

Genetics of Charcot Marie Tooth (CMT) - Modifiers of CMT1A, New Causes of CMT2

Studying Autosomal dominant Charcot-Marie-Tooth disease type 2

Last synced from ClinicalTrials.gov

Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing data

Key facts

Sponsor
University of Iowa
Principal Investigator
Michael E Shy, MD
University of Iowa
Enrollment
1050 enrolled
Eligibility
All sexes
Timeline
20102026

Study locations (22)

Collaborators

National Institute of Neurological Disorders and Stroke (NINDS) · Muscular Dystrophy Association · University of Rochester · University of Pennsylvania · King's College Hospital NHS Trust · Sydney Children's Hospitals Network · Children's Hospital of Philadelphia · University of Miami · Johns Hopkins University · Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta · Cedars-Sinai Medical Center · Nemours Children's Clinic · Stanford University · University of Minnesota · Massachusetts General Hospital · University of Colorado, Denver · Children's National Research Institute · University of Michigan · St. Jude Children's Research Hospital · Connecticut Children's Medical Center · Seattle Children's Hospital · The Hospital for Sick Children

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT01193088 on ClinicalTrials.gov

Other trials for Autosomal dominant Charcot-Marie-Tooth disease type 2

Additional recruiting or active studies for the same condition.

See all trials for Autosomal dominant Charcot-Marie-Tooth disease type 2

← Back to all trials