The Dose Finding Study of DAOIB Added to tDCS for AD

Status Suspended

Clinical Trial Summary

This is a 26-week randomized, double-blind, placebo-controlled trial. We will enroll patients with aMCI or mild AD. All patients will receive 2 weeks of tDCS (5 sessions per week, 10 sessions in total) during the first 2 weeks of the study, and will also be allocated randomly to either of 4 treatment groups for 24 weeks: (1) Dose A group; (2) Dose B group; (3) Dose C group; (4) placebo group. We will assess the patients every 8 weeks during the treatment period (weeks 0, 10, 18, and 26). We hypothesize that augmentation with certain dose of DAOIB will yield better effect than tDCS alone in improving the cognitive function, global functioning and quality of life in patients with aMCI or mild AD.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Dementia
Transcranial Direct Current Stimulation

Clinical Trial Details

NCT number	NCT05006781
Study type	Interventional
Source	Chang Gung Memorial Hospital
Contact
Status	Suspended
Phase	Phase 2
Start date	January 2025
Completion date	December 2027

View Details

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