Objective: Evaluation the improvement of the cognitive function of tandospirone add-on treatment on patients with AD comorbid anxiety. Number of Patients: 30 Methodology: Randomized, open-label, parallel-group Assigned Interventions: Experimental: Tandospirone, 30-60 mg/d + Donepezil, 10 mg/d; Control group: Donepezil, 10 mg/d. Effect Evaluation: Primary Outcome: Change from baseline in ADAS-cog total score at week 12; NPI scale total score at week 12;
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Tandospirone, 30-60 mg/d
Donepezil, 10 mg/d
Change of ADAS-cog total score
Change from baseline in ADAS-cog total score at week 12
Time frame: week 12
NPI scale total score
NPI scale total score at week 12
Time frame: week 12
HAMA total score
HAMA total score at week 12
Time frame: week 12
FAB score
FAB score at week 12
Time frame: week 12
relative power
Change from baseline in the relative power at week 12
Time frame: week 12
the image of PET
the image of PET at week 12
Time frame: week 12
MMSE score
MMSE score at week 12
Time frame: week 12
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