Clin2
NCT04880356Possibly a fitRecruiting

Study of very rare inherited brain diseases over time

Inherited DiseaseRare DiseasesMetabolic DiseaseUndiagnosed DiseaseNeurologic DisorderNeuro-Degenerative Disease

Part of Brain & nervous system, Cancer, Digestive system, Genetic & congenital, Hormones & metabolism clinical trials.

This study follows adults over time who have a very rare inherited brain disease, or whose illness seems like it may run in families. The goal is to better understand these conditions and how they progress.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
100 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You must be at least 18 years old
  • You have a very rare inherited brain (neurologic) disease or symptoms
  • Your condition is thought to be inherited in your family, or it’s still not diagnosed
  • There are no stated study exclusions in the criteria provided

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT07527624Recruiting
Study of work and social inclusion for young adults with rare genetic conditions

This study looks at how young adults aged 15–25 with rare genetic conditions (like certain bone, skin, hearing, or facial conditions) are doing in school, work, and social life. Researchers want to understand what helps or prevents young people with these conditions from being included in their communities.

Paris, Île-de-France Region
NCT01143454Recruiting
Study unusual heart conditions and related genetic traits

This study looks at people with unusual or rare heart problems, or people with a family history of these issues. Doctors and researchers may collect and study your blood or tissue (and possibly store samples) to learn what causes the condition and how it may affect the heart.

Washington D.C., District of Columbia
NCT04703179Enrolling by invitation
Rare disease and undiagnosed case research blood and tissue biobank

This study collects and stores samples and related medical information for people with rare diseases or suspected genetic conditions. It may help researchers better understand these conditions and develop future testing and treatments.

Scottsdale, Arizona
NCT07714161Enrolling by invitation
Mayo Clinic study for rare and undiagnosed conditions

This study brings together experts to try to find answers for people with rare or undiagnosed conditions. If standard genetic tests haven't given you a diagnosis, this research may help uncover new clues.

Rochester, Minnesota
NCT05499091Recruiting
Study rare disease genetics using family and health data

This study tries to find genetic causes for rare diseases that are not yet understood. It uses a national rare-disease data bank and collects consent from patients and sometimes close family members.

Angers
NCT01793168Recruiting
Rare disease registry and history study

This study keeps a registry (a structured list) of people with rare diseases and may also track how the condition changes over time. It can help researchers better understand rare illnesses and find gaps in care, which may improve future treatments.

Sioux Falls, South Dakota

Hear when a new Inherited Disease trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.