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Randomized Clinical Trial; the effect of Bangle Rhizome on mild cognitive impairment

Randomized Clinical Trial; the effect of Bangle Rhizome on mild cognitive impairment - RCT Bangle Rhizomeon MCI

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000045946
Enrollment
60
Registered
2021-11-01
Start date
2021-11-01
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

healthy elderly with MCI

Interventions

Bangle Rhizome 600 mg/day Bangle Rhizome 300mg/day placebo

Sponsors

Tokushima University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Elderly people who are healthy and maintain their daily activities, but have mild cognitive decline, and who have given their consent to the study. Persons with an MMSE rating of 24 points or more and 27 points or less Organ function: Those who do not find any obvious abnormal values in blood tests

Exclusion criteria

Exclusion criteria: (1) Persons suffering from serious cerebrovascular disease, heart disease, liver disease, renal disease, gastrointestinal disease, infectious disease requiring notification, etc. (2) Those who are diagnosed with overt dementia (3) Chronic diseases (diabetes, heart disease, liver failure, renal failure, gastric / duodenal ulcer, colitis, Those who are being treated or taking medication due to Crohn's disease, cancer, etc.) (4) Persons with significant abnormalities in blood pressure measurement and blood test (5) Persons with severe anemia, malnutrition, or bleeding tendency (6) Those who frequently have diarrhea symptoms (7) Persons who may show allergic symptoms to the subject (8) Excessive smoking and alcohol addicts and those with extremely irregular lifestyle habits such as eating and sleeping (9) Those who are currently participating in other clinical trials or who have participated within one month (10) Others who are judged to be ineligible by the tester

Design outcomes

Primary

MeasureTime frame
Cognitive function evaluation

Secondary

MeasureTime frame
Changes in oral bacterial flora, taste threshold, dietary intake, ADL assessment

Countries

Japan

Contacts

Public ContactRie Tsutsumi

Tokushima University Department of Metabolism and Nutrition

rtsutsumi@tokushima-u.ac.jp81-88-633-9249

Outcome results

None listed

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