ClinicaliQ Trial Snapshot
- Genetics of Charcot Marie Tooth (CMT) – Modifiers of CMT1A, New Causes of CMT2 — Recruiting • NCT01193088.
- Research identifying new CMT-causing genes and genes that modify disease severity in CMT patients.
Verify eligibility, endpoints and current status on the original ClinicalTrials.gov registry before acting on this summary.
Use This Page For
- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
- Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying
This project includes two projects. One is looking for new genes that cause Charcot Marie Tooth disease (CMT). The other is looking for genes that do not cause CMT, but may modify the symptoms a person has. Conditions: Charcot-Marie-Tooth Disease, Type Ia (Disorder), HMSN Lead Sponsor: University of Iowa Planned Enrollment: 1050 participants