No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
21 – 75
Sex
Any
Study type
Observational
Participants needed
30 (estimated)
Sponsor
University of Minnesota · Other
Who this trial is looking for
This trial is looking for people with amyotrophic lateral sclerosis (ALS), primary lateral sclerosis (PLS), or healthy individuals to participate in MRI scans. Researchers want to find measurable signs of these diseases.
Are You a Good Fit for This Trial?
You may be able to join if
I am between 21 and 75 years old.
I am able to give signed consent for the study.
I have been diagnosed with ALS or PLS.
You may not be able to join if
I have another neurodegenerative disease like Parkinson's or Alzheimer's.
I have had a serious unstable medical illness in the last 30 days.
I cannot stay still in an MRI machine for more than 30 minutes.
I have a pacemaker or other devices in my body that are not allowed during an MRI.
I weigh more than 300 lbs.
I cannot comfortably lie flat for 75-90 minutes.
I need help walking or climbing stairs, and I am not expected to improve in the next year.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
The purpose of the study is to determine if we are able to find one or more biomarkers of Amyotrophic Lateral Sclerosis (ALS) and Primary Lateral Sclerosis (PLS) using magnetic resonance imaging (MRI) scans at different levels, 3 tesla (3T) and 7 tesla (7T). A biomarker is a measurable characteristic that can be used as an indicator of a particular disease state. Identifying biomarkers of a diseas…
The purpose of the study is to determine if we are able to find one or more biomarkers of Amyotrophic Lateral Sclerosis (ALS) and Primary Lateral Sclerosis (PLS) using magnetic resonance imaging (MRI) scans at different levels, 3 tesla (3T) and 7 tesla (7T). A biomarker is a measurable characteristic that can be used as an indicator of a particular disease state. Identifying biomarkers of a disease can lead to a better understanding of the disease as well as improved treatments. This study will enroll patients with ALS, PLS, and healthy controls.
Trial Locations
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Status
Eligibility Criteria
Inclusion Criteria:
* 21 to 75 years of age inclusive.
* Willing and able to give signed informed consent that has been approved by the Institutional Review Board (IRB).
ALS patients:
* A clinical diagnosis of possible, laboratory-supported probable, probable, or definite ALS, according to a modi…
Inclusion Criteria:
* 21 to 75 years of age inclusive.
* Willing and able to give signed informed consent that has been approved by the Institutional Review Board (IRB).
ALS patients:
* A clinical diagnosis of possible, laboratory-supported probable, probable, or definite ALS, according to a modified El Escorial criteria.
Exclusion Criteria:
* Diagnosis of other neurodegenerative diseases (Parkinson disease, Alzheimer disease, etc).
* Clinically significant history of unstable medical illness (unstable angina, advanced cancer, etc) over the last 30 days.
* Inability to undergo MRI scanning, including but not limited to unable to remain still in an MRI scanner for more than 30 minutes, claustrophobia, presence of paramagnetic substances or pacemakers in body, weight over 300 lbs, or in the opinion of the investigator, if there is a strong likelihood that the subject would not be able to lie flat comfortably for 75-90 minutes.
* The subject requires assistance to ambulate OR climb stairs, unless in the opinion of the investigator, and based upon the subject's rate of disease progression, the subject is likely to be able to participate in the MRI screening 12 months after enrollment.
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