NCT03639285

Natural History, Diagnosis, and Outcomes for Leukodystrophies

• Status: Recruiting
• Phase: —
• Study type: Observational
• Enrollment: 600 (estimated)
• Sponsor: University of Utah · Academic / Other
• Sex: All
• Age: —
• Healthy volunteers: Not accepted

Summary

The goals of this protocol is to diagnose, care for, and understand the clinical histories and outcomes of people with leukodystrophies.

Detailed description

Inherited leukodystrophies affect close to 1 in 7500 children with mortality greater than 30%. Affected patients face additional serious medical complications including epilepsy, developmental regression, and intellectual disabilities. Diagnosis is difficult and requires the assistance of a specialist. Finally, identifying treatments and improving outcomes is complex. The Western Leukodystrophy Project, which is part of the University of Utah and of Primary Children's Hospital, and which is a certified Leukodystrophy Care Network Center, provides a specialized resource for patients with leukodystrophies. This clinical study assists with diagnosis of leukodystrophies; suggesting treatment options and implementing care guidelines, and improving outcomes for all patients by understanding the clinical histories and outcomes of affected patients..

Conditions

• Leukodystrophy

Timeline

• Start date: 2007-01-19
• Primary completion: 2033-12-31
• Completion: 2050-12-31
• First posted: 2018-08-21
• Last updated: 2026-01-13

Locations

1 site across 1 country: United States