Browse Studies — Arctuva

WiTNNess: An International Natural History Study of Autosomal Recessive TNNT1 Myopathy

WiTNNess is designed to accurately document the natural course and variation of muscle disease caused by pathogenic changes of the TNNT1 gene. The primary aim …

TNNT1-associated MyopathyInfantile-onset Nemaline Rod MyopathyMyopathies, Nemaline+9 more

Estimated

~$10 – $750

Clinic for Special ChildrenNCT06374719

Observational

Effects of Whole-body Electrical Muscle Stimulation Exercise on Adults withNeuromuscular Disease

This single-arm pilot study evaluates the effects of whole-body electrical muscle stimulation (WB-EMS) exercise on neuromuscular and physical function in adult…

Neuromuscular Diseases (NMD)Amyotrophic Lateral SclerosisMyasthenia Gravis+15 more

Estimated

~$10 – $6,250

University of Missouri-ColumbiaNCT07478172

Nemaline Myopathy Clinical Research Network (NM-CTRN)

The goal of this study is to establish a research network to help define the natural disease history and clinical outcome measures for Nemaline Myopathy (NM).

Nemaline Myopathy

Estimated

~$10 – $750

Stanford UniversityNCT06774703

Molecular Analysis of Neuromuscular Disease

In the Congenital Myopathy Research Program at Boston Children's Hospital and Harvard Medical School, the researchers are studying the congenital myopathies (n…

Central Core DiseaseCentronuclear MyopathyCongenital Fiber Type Disproportion+5 more

Estimated

~$10 – $750

Boston Children's HospitalNCT00272883