Efficacy Biomarkers of DAOIB for Dementia
Condition(s) studied
Investigational drug(s) / intervention(s)
DAOIB: The DAOIB dose will be adjusted every 8 weeks according to clinical evaluation.
Study summary
This open-label clinical trial will enroll patients with aMCI or mild AD, and they will be treated with DAOIB for 24 weeks. We will assess the patients before entering the study, 8 weeks, 16 weeks, and end point (24 weeks) of the study, and measure blood NMDA and oxidative stress - related biomarkers every 8 weeks. We hypothesize that NMDA and oxidative stress - related biomarkers can predict the efficacy of DAOIB for patients with aMCI or mild AD.
Eligibility
Primary outcome measure(s)
- Change from baseline in the Alzheimer's disease assessment scale - cognitive subscale at week 8, 16 and 24 — week 0, 8, 16, 24
Alzheimer's disease assessment scale-cognitive subscale scores range from 0 (best) to 70 (worst)
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Chang Gung Memorial Hospital | Kaohsiung City | Taiwan | Recruiting |
| China Medical University Hospital | Taichung | Taiwan | Recruiting |
More Chang Gung Memorial Hospital trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05582161 on ClinicalTrials.gov ↗ ← All trials in China