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The study of ALS biomarker based on molecular dynamics of oxidative stress regulatory factor

The study of ALS biomarker based on molecular dynamics of oxidative stress regulatory factor - ALS biomarker research

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000013245
Enrollment
60
Registered
2014-02-25
Start date
2013-09-11
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Amyotrophic lateral sclerosis Parkinson&#39

Interventions

None listed

Sponsors

Faculty of Medicine, Kitasato University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients diagnosed as having ALS and satisfying all of the following criteria. 1)ALS patients who are diagnosed by EL Escorial revised Airlie House criteria as clinically definite,clinically probable or clinically probable-laboratory-supported, clinically pssible ALS or clinically suspected ALS, and Stage I, II or III in ALS severity classification. 2)Older than 20 and younger than 71 years old 3)Patients who give informed consent after detailed explanation of the study As disease controls, PD or MS patients satisfying all of the following criteria. 1)Older than 20 and younger than 71 years old 2)Patients who consulted a nerve outpatient and obtained consent for study entry 3)Patients who give informed consent after detailed explanation of the study Healthy individuals satisfying all of the following criteria. 1)Older than 20 and younger than 71 years old 2)Healthy individuals who have interest in this study 3)Healthy individuals who give informed consent after detailed explanation of the study

Exclusion criteria

Exclusion criteria: 1)Patient to whom the diagnosis has not been disclosed 2)Patient having severe psychiatric symptoms (hallucination, delusion) or dementia 3)Patient having serious orthostatic hypotension or other types of hypotension 4)Patient having a severe complication(s) such as heart, kidney and/or liver disease 5)Patient having the complications of the allergic disease that an acidophile level is easy to rise 6)Patient did not have ability to comprehend informed consent 7)Patient who was inappropriate for this study 8)Patient who has received an investigational drugs or devices within three months before 9) Patient who participates in other clinical trials *The patient treated with existing therapeutic drug does not correspond to exclusion criteria

Design outcomes

Primary

MeasureTime frame
Exploration of novel biomarker

Countries

Japan

Contacts

Public ContactKazunori Tanaka

Faculty of Medicine, Kitasato University Department of Molecular Neurology

alspd@med.kitasato-u.ac.jp042-778-9441

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026