1200 Participants Needed

Research Procedures for ALS

(CAPTURE-ALS Trial)

Recruiting at 12 trial locations
MB
SH
AG
JH
Overseen ByJessica Hernandez
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: University of Miami
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

The trial aims to learn more about amyotrophic lateral sclerosis (ALS) and related disorders by collecting and studying information from patients' medical records. ALS affects nerve cells in the brain and spinal cord, leading to muscle weakness and movement problems. The trial includes clinical procedures that gather data to help researchers better understand the disease. Suitable candidates include those diagnosed with ALS or a similar disorder, receiving care at a clinic using Epic for electronic health records, and able to give informed consent or have a proxy to do so. As an unphased trial, this study offers a unique opportunity to contribute to the foundational understanding of ALS and related disorders.

Do I need to stop my current medications for the trial?

The trial information does not specify whether you need to stop taking your current medications.

Why are researchers excited about this trial?

Researchers are excited about the clinical procedures being explored for ALS because they aim to uncover novel insights into the disease's progression and response to interventions. Unlike standard treatments that focus on symptom management or slowing disease progression, these procedures could lead to breakthroughs in understanding the underlying mechanisms of ALS. By refining diagnostic techniques or exploring new intervention strategies, this research could pave the way for more effective and targeted therapies in the future.

Who Is on the Research Team?

MB

Michael Benatar, MBChB, MS, DPhil

Principal Investigator

University of Miami

Are You a Good Fit for This Trial?

Inclusion Criteria

Diagnosis of ALS or a related disorder (e.g. primary lateral sclerosis, progressive muscular atrophy).
Receiving care at a clinical center that uses Epic as its EHR.
Able and willing to provide informed consent (or informed consent obtainable from a designated proxy).

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Data Collection

Systematic gathering of clinical data through the EHR to characterize the natural history of ALS and related diseases

Ongoing

Follow-up

Participants are monitored for safety and effectiveness after data collection

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Clinical Procedures

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Miami

Lead Sponsor

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976
Recruited
423,000+

National Center for Advancing Translational Science (NCATS)

Collaborator

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100
Recruited
32,100+

Muscular Dystrophy Association

Collaborator

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38
Recruited
60,800+

National Institute of Neurological Disorders and Stroke (NINDS)

Collaborator

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1,403
Recruited
655,000+

National Center for Advancing Translational Sciences (NCATS)

Collaborator

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394
Recruited
404,000+

National Institutes of Health (NIH)

Collaborator

Trials
2,896
Recruited
8,053,000+
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