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NCT06528964Recruiting

Proteinopathies Expression in Skin of Neurodegenerative Disorders

Expression of Proteinopathies in Skin Biopsies of Patients With Neurodegenerative Disorders

Source: ClinicalTrials.gov · Last updated 16 Dec 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The goal of this observational study is to compare the aggregation pattern of proteinopathies (alpha-synuclein, amyloid-beta, phosphorylated tau and transactive response DNA -binding protein 43 \[TDP43\]) in skin biopsies of patients with a neurodegenerative disease like Alzheimer's disease, frontotemporal lobe dementia, Parkinson's disease, atypical Parkinsonism, amyotrophic lateral sclerosis or normal pressure hydrocephalus. The main question it aims to answer is: * Is there a specific pattern of aggregation of proteinopathies in skin biopsies in each neurodegenerative disease in comparison to healthy control subjects? Skin biopsies will be analyzed using immunohistochemistry and immunofluorescence for detection of alpha-synuclein, amyloid-beta, phosphorylated tau and TAR DNA binding protein 43, and the aggregation patterns will be compared between patients with a neurodegenerative disease vs patient with normal pressure hydrocephalus vs healthy control subjects.

Status (registry)
Recruiting
Study type
Observational
Enrollment
40 (estimated)
First submitted
25 Jul 2024
Start date
20 Dec 2023
Primary completion date
25 Oct 2026
Lead sponsor
Universidad Autonoma de San Luis Potosí
NCT number
NCT06528964

What you commit to

  • Study type: Observational
  • Planned participants: 40
  • From 20 Dec 2023 to the primary completion date, 25 Oct 2026
  • 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 illness

  • Patients or controls that have a personal history of cerebrovascular disease, psychiatric disease, post traumatic dementia or HIV related dementia
  • Patients or controls that a diagnosed skin disease
  • Patients that have an "atypical" presentation of the disease

Other

  • Patients in which the diagnosis is not clear or hasn't been confirmed
  • Patients or controls that have a neuroinfection
  • Patients or controls that have diagnosis of a coagulopathy

Who the study is looking for

  • Patients 45 years and older
  • Men and women
  • Patients diagnosed with Alzheimer's disease, frontotemporal lobe dementia, Parkinson's disease, atypical Parkinsonism, amyotrophic lateral sclerosis or normal pressure hydrocephalus
  • Patients that voluntarily accept to participate in the study and accept the consent form
  • People 45 years and older
  • Men and women
  • Subjects can be related to a patient but not by blood (for example spouse of a patient)
  • Subjects don't have direct family history of a neurodegenerative control
  • Subjects don't have any clinical findings suggesting dementia
  • Subjects voluntarily accept to participate in the study and accept the consent form

Age in the registry: 45 years to - · Sex: All · Accepts 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
Hospital Central Dr. Ignacio Morones Prieto
Coordinator of this site? Confirm its status
San Luis Potosí CityMexicoRecruiting

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