drugset / Trial / NCT03151382
A Based on PEEG and PET Study of Anxiolytic Treatment to Improve Cognitive Function in Patients With Alzheimer Disease
RandomizedParallel-groupOpen-labelTreatment
Summary
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;
Timeline
- Start
- 2017-05-20
- Primary completion
- 2017-12-31
- Completion
- 2018-06-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tandospirone | Small molecule | 30 mg | — |
| Subject | Tandospirone | Small molecule | 60 mg | — |
| Background | Donepezil | Small molecule | 10 mg | — |