drugset / Trial / NCT03151382

A Based on PEEG and PET Study of Anxiolytic Treatment to Improve Cognitive Function in Patients With Alzheimer Disease

NCT03151382

Phase 4 Unknown 30 enrolled Zhejiang Provincial People's Hospital
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

EvaluationDrugModalityDoseRoute
Subject Tandospirone Small molecule 30 mg
Subject Tandospirone Small molecule 60 mg
Background Donepezil Small molecule 10 mg

Indications