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NCT04880356Recruiting

Longitudinal Study of Ultra-rare Inherited Metabolic and Degenerative Neurological Diseases.

Clinical, Instrumental and Laboratory Data Collection of Subjects with Ultra-rare Inherited Metabolic and Degenerative Neurological Diseases

Source: ClinicalTrials.gov · Last updated 19 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

General aim of the study is the improvement of the clinical knowledge of ultra-rare inherited metabolic and degenerative neurological diseases (prevalence less than 5:100,000) in adulthood through the systematic longitudinal collection of clinical, laboratory and instrumental data.

Status (registry)
Recruiting
Study type
Observational
Enrollment
100 (estimated)
First submitted
19 Apr 2021
Start date
1 Mar 2021
Primary completion date
31 Mar 2031
Lead sponsor
Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta
NCT number
NCT04880356

What you commit to

  • Study type: Observational
  • Planned participants: 100
  • From 1 Mar 2021 to the primary completion date, 31 Mar 2031
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • none

Who the study is looking for

  • Age \>= 18 years
  • Subjects with ultra-rare inherited degenerative and metabolic neurological diseases
  • Subjects with undiagnosed neurological diseases (when supposed to be inherited)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Fondazione IRCCS Istituto Neurologico Carlo Besta
Coordinator of this site? Confirm its status
MilanItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.