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Placebo controlled double blind randomized Phase II Clinical Trial of sodium pyruvate on lactic acidosis associated with mitochondrial disorders

Placebo controlled double blind randomized Phase II Clinical Trial of sodium pyruvate on lactic acidosis associated with mitochondrial disorders - Lactic acidosis associated with mitochondrial disorders, intervention by sodium pyruvate

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1091220093
Enrollment
12
Registered
2012-07-24
Start date
2016-06-07
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

lactic acidosis associated with mitochondrial disorders

Interventions

Intervention type:DRUG Name of intervention:sodium pyruvate Dose form / Japanese Medical Device Nomenclature:GRANULES Route of administration / Site of application:ORAL,ORAL,ORAL Dose per administrati

Sponsors

Yasutoshi Koga Department of Pediatrics and Child Health, Kurume University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: mitochondrial disease who fulfilled the following criteria 1) patient whoes age is over than 6 years-old 2) patient who are fulfilled the diagnostic criteria of MELAS/MELA 3) patientwho has an A3243G mutation. 4) no past history of sodium pyruvate administration for the therapeutic purpose 5) patient whose score of section 1+2 by JMDRS is more than 10, and one of the specific score is more than 2. 6) patient who have a written informed conscent or ascent by his/her own opinion.

Exclusion criteria

Exclusion criteria: 1) patient who has bed ridden status 2) patient who has dementic status and cannot be evaluated the JMDRS/NMDAS by medical doctor 3) patient who has uncontrolled status epileptics 4) patient who has septic status 5) patient who has renal failre, and less than 60mL/min/1.73m by eGFR 6) patient who has hypertrophic cardiomyopathy or cardiac failre 7) patient who has allergic state against sodium pyruvate 8) patient who enrolled to the other clinical trial within 6 months 9) patient who has pregnant 10) patient who is not recommended to the entry by medical doctor

Design outcomes

Primary

MeasureTime frame
JMDRS section 1 & 2

Secondary

MeasureTime frame
NMDAS section 1-3, brain lactate by MRS, GDF15

Countries

Japan

Contacts

Public ContactYasutoshi Koga

Kurume University School of Medicine

yasukoga@med.kurume-u.ac.jp+81-942-31-7565

Outcome results

None listed

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