Unique ID issued by UMIN | UMIN000037839 |
---|---|
Receipt number | R000043042 |
Scientific Title | A study of usefulness of plasma lyso-GL-3 as a biomarker in patients with Fabry disease |
Date of disclosure of the study information | 2019/09/01 |
Last modified on | 2024/12/18 11:25:00 |
A study of usefulness of plasma lyso-GL-3 as a biomarker in patients with Fabry disease
Plasma lyso-GL-3 in patients with Fabry disease
A study of usefulness of plasma lyso-GL-3 as a biomarker in patients with Fabry disease
Plasma lyso-GL-3 in patients with Fabry disease
Japan |
Fabry disease
Cardiology | Nephrology | Pediatrics |
Laboratory medicine |
Others
NO
The aim of the study is to confirm the usefulness of plasma lyso-GL-3 as an effective bio-marker for Fabry disease patients not only for diagnosis but also to confirm their clinical conditions by comparing collected data of the value and its change in Japanese Fabry disease patients between plasma lyso-GL-3, plasma GL-3 which is already used for diagnosis of male Fabry disease patients, and tests values and change of renal function and heart function by which clinical symptoms are observed in Fabry disease patients.
Others
The usefulness of plasma lyso-GL-3 as a bio-marker for condition management in patients with Fabry disease.
To investigate correlation between plasma lyso-GL-3 and clinical features as follows; Plasma GL-3, eGFR, Urinary protein-to-creatinine ratio, BNP, LV mass index, EF, Presence of cardiac hypertrophy, Urinary mulberry body
Observational
Not applicable |
Not applicable |
Male and Female
1) Patients who were diagnosed as Fabry disease and meet the following criteria.
Male
-Male patients who can be diagnosed as having Fabry disease by their enzyme activities.
Female
-Female patients who can be diagnosed by genetic test or genetically confirmed (family history) as having Fabry disease. And, can be diagnosed as Fabry disease by decrease of enzyme activities or clinical presentation.
2) Patients who are receiving, or scheduled to receive enzyme replacement therapy with agalsidase beta BS.
3) Patients who are fully informed of and understand about the study and provide the written consent to participate in the study by themselves or their representatives. (For minor patients aged 16 years or older at informed consent, consent generally should be obtained from themselves.)
1) Patients who received before, are receiving now or are scheduled to receive Hematopoietic Stem Cell Transplantation / Chaperone therapy.
2) Patients who are considered as ineligible for the study by the investigator.
100
1st name | Norio |
Middle name | |
Last name | Sakai |
Osaka University Graduate School of Medicine, Division of Health Science
Child Healthcare and Genetic Science Laboratory
565-0871
1-7 Yamadaoka, Suita, Osaka
06-6879-2531
norio@sahs.med.osaka-u.ac.jp
1st name | Norio |
Middle name | |
Last name | Sakai |
Osaka University Graduate School of Medicine, Division of Health Science
Child Healthcare and Genetic Science Laboratory
565-0871
1-7 Yamadaoka, Suita, Osaka
06-6879-2531
norio@sahs.med.osaka-u.ac.jp
Osaka University Graduate School of Medicine, Division of Health Science, Child Healthcare and Genetic Science Laboratory
JCR Pharmaceuticals Co., Ltd.
Profit organization
Translational Research Center for Medical Innovation, Foundation for Biomedical Research and Innovation at Kobe
Osaka University Clinical Research Review Committee
2-2 Yamadaoka, Suita, Osaka, Japan
06-6210-8296
rinri@hp-crc.med.osaka-u.ac.jp
NO
国立大学法人大阪大学医学部附属病院
国立大学法人岐阜大学医学部附属病院
大阪市立大学医学部附属病院
独立行政法人国立病院機構関門医療センター
埼玉医科大学病院
2019 | Year | 09 | Month | 01 | Day |
Unpublished
No longer recruiting
2019 | Year | 05 | Month | 21 | Day |
2019 | Year | 07 | Month | 31 | Day |
2019 | Year | 09 | Month | 01 | Day |
2025 | Year | 03 | Month | 31 | Day |
Publication of results:
Unpublished, Partially published, Published
2019 | Year | 08 | Month | 29 | Day |
2024 | Year | 12 | Month | 18 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000043042