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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

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

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