drugset / Trial / NCT03728153

Measuring Ambulation, Motor, and Behavioral Outcomes With Post-Stroke Fluoxetine in Tanzania

NCT03728153

NaSingle-groupOpen-labelTreatment

Summary

This is a phase II, randomized study of 120 adults age 18 or above who will prescribed 20mg daily Fluoxetine for 90 days following acute, ischemic stroke.

Timeline

Start
2019-11-26
Primary completion
2021-01-06
Completion
2021-01-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Fluoxetine Small molecule 20 mg Oral

Indications