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A clinical study for patients with moderate to severe Alzheimer's disease using Memantine hydrochloride OD tablet.

A clinical study for patients with moderate to severe Alzheimer's disease using Memantine hydrochloride OD tablet. - A clinical study for patients with moderate to severe Alzheimer's disease using Memantine hydrochloride OD tablet.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000014581
Enrollment
60
Registered
2014-07-22
Start date
2014-08-22
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&#39

Interventions

Switching from Memantine hydrochloride tablet 20mg to Memantine hydrochloride OD tablet 20mg Intervention period of 4 weeks

Sponsors

Enomoto naika clinic
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients who are diagnosed as moderate to severe Alzheimer's disease by investigator 2.Patients who have taken Memantine hydrochloride tablet 20mg for 4 weeks before evaluation period 3.Patients who are 20 years or over 4.Patients who are able to understand this study and give informed consent in literature by patient and a caregiver or families

Exclusion criteria

Exclusion criteria: 1.Dementia patients except Alzheimer's disease 2.Patients who have severe mental disorder 3.Patients who are pregnant or trying to get pregnant, or during breastfeeding 4.Patients with a history of the hypersensitivity for Memantine hydrochloride tablets 5.The case that a investigator judged to be inappropriate

Design outcomes

Primary

MeasureTime frame
Evaluation of functionality

Secondary

MeasureTime frame
Evaluation of safety

Countries

Japan

Contacts

Public ContactHiroki Kato

Sogo Rinsho Medefi Company Limited Business Promotion Department

kato.hiroki@sogo-medefi.jp03-6901-6079

Outcome results

None listed

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