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The effects of the electrolyzed calcium on Alzheimer's Disease

Study of the effects of the electrolyzed calcium on behavioral and psychological symptoms of dementia due to Alzheimer's Disease

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs031200068
Enrollment
18
Registered
2020-07-16
Start date
2020-09-10
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

Alzheimer's Disease Behavioral and psychological symptoms of dementia

Interventions

Tachikawa electrolyzed calcium given on twice daily for 24 weeks followed, until disease progression or unmanageable toxicity

Sponsors

Homma Sadamu
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) At least one Neuropsychiatric Inventory-Questionnaire score more than 2 2) Probable Alzheimer's Disease dementia in the criteria by National Institute of Neurological and Communicative Disorders and Stroke AD and Related Disorders Association 3) Compatible with 2) during the observation one month prior to the start of the drug administration 4) Over 60 years old 5) Male and Female (Both) 6) Agreement by the legal representative 7) Certain performance of the treatment and observation based on the study schedule 8) No matter about the intake of other calcium drug types 9) Normal or low serum calcium level, and in case of hypoalbuminemia, calculate and judge corrected calcium level.

Exclusion criteria

Exclusion criteria: 1) Severe damage of hepatic, renal, and cardiovascular function (According to CTCAE version 5.0, Grade 3) 2) Malignant neoplasms 3) History of severe drug allergy such as anaphylaxic reaction or severe drug side effects 4) Intake of the unapproved anti-dementia drug for the medical test within 12 weeks prior to the agreement with this study 5) Pregnancy certain or possible 6) Breastfeed 7) Inadequate to enroll in this study judged by the chief or co-investigator

Design outcomes

Primary

MeasureTime frame
Neuropsychiatric InventryInventory-Questionnaire

Secondary

MeasureTime frame
Dementia Behavior Disturbance Scale

Contacts

Public ContactSadamu Homma

Soujinkai Hospital

hommas@live.jp+81-297-85-8341

Outcome results

None listed

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