Plain-English translation of NCT07175935 on ClinicalTrials.gov โ ยท Source last updated ยท Translation generated ยท How we translate trials
This is a research study that follows people diagnosed with ALS over time. Researchers are building a database of information from ALS patients across Thailand to better understand how the disease progresses, what genetic factors may be involved, and how it affects quality of life. No experimental medications or treatments are being tested โ you'll receive your normal medical care while researchers collect information.
Thailand currently doesn't have large-scale organized information about ALS patients โ how common it is, what it looks like in Thai patients, genetic patterns, and long-term outcomes. This database will help doctors and researchers understand ALS better and eventually develop better treatments and care plans for people living with the disease.
You likely qualify ifโฆ
You likely don't qualify ifโฆ
You would visit one of the participating hospitals or neuromuscular clinics for regular appointments where researchers collect information about your health using standardized assessments. These visits may include tests of muscle strength, breathing function, and quality-of-life questionnaires. Your medical information is stored securely in a database. You continue receiving your regular ALS care from your own doctors throughout the study.
AI-generated summary from trial data ยท Jun 1, 2026 ยท Not medical advice
Thailand
~100 participants
Started
March 2025
Primary completion
December 2030
Last updated on clinicaltrials.gov in September 2025.
Reach out to the team running this trial. Response times vary โ some teams are faster than others.
Central contact
Jakkrit Amornvit, MD
Chulalongkorn University
Tell us you're interested and we'll help connect you with the research team. We'll walk you through what to expect first โ no email needed to get started.