Analysis of ALS patient tissues and registry

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This research focuses on understanding Amyotrophic Lateral Sclerosis (ALS) by collecting data from patients through physical examinations, electrodiagnostic testing, and MRI scans. Patients will consent to have their information entered into a database to monitor disease progression and contribute to research efforts. Additionally, a separate consent will allow for postmortem tissue collection to facilitate in-depth cellular and molecular analyses. The goal is to identify reliable markers of disease progression and potential treatment avenues.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients over the age of 18
* Established diagnosis of ALS
* Able and willing to give written informed consent and must authorize release and use of protected health information

Exclusion Criteria:

* Patients below the age of 18
* No diagnosis of ALS

Where it's running

• University of Illinois at Chicago
  Chicago, Illinois, United States Recruiting

Study contacts

• Principal investigator: Jeffrey Loeb, MD — University of Illinois Chicago
• Study coordinator: Ayo Fasawe
• Email: afasawe@ilstu.edu
• Phone: 312-413-7908

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.