Skip to content

Effects of Kleeb Bua Daeng Formula on Changes in Biomarkers among Patients with Mild Cognitive Impairment: A Pilot Study for a Randomized Clinical Trial

Effects of Kleeb Bua Daeng Formula on Changes in Biomarkers among Patients with Mild Cognitive Impairment: A Pilot Study for a Randomized Clinical Trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250204007
Enrollment
10
Registered
2025-02-04
Start date
2025-02-28
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

mild cognitive impairment Kleeb Bua Daeng, mild cognitive impairment

Interventions

2 capsules 2 times a day for 90 days,2 tablets once a day
Experimental Drug,Active Comparator Drug
kbd,egb

Sponsors

CHAO PHYA ABHAI BHUBEJHR hospital foundation
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Age 60 to 75 years 2.Diagnosed with Mild Cognitive Impairment based on standard criteria with a MoCA score of 19 to 24 points. 3.Willing to participate in the study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. History of allergy to any herbal components in the Kleeb Bua Daeng formula. 2. History of other neurological disorders such as Parkinson's disease Lewy body dementia epilepsy schizophrenia or bipolar disorder. 3. Participation in another research study within the past 30 days meaning volunteers must not be enrolled in any other research projects for at least 30 days prior to joining this study. 4. Currently receiving Alzheimer disease medications or drugs that significantly affect the central nervous system.

Design outcomes

Primary

MeasureTime frame
MoCA score 90 days MoCa test

Secondary

MeasureTime frame
AST ALT eGFR 90 days blood sample test

Countries

Thailand

Contacts

Public ContactNatdanai Musigavong

ministry of public health

mus_natda@kkumail.com0892055606

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026