drugset / Trial / NCT03350659

Efficacy and Safety of Midodrine and Atomoxetine for Neurogenic OH

NCT03350659

RandomizedParallel-groupOpen-labelTreatment

Summary

This was a randomized, open-label clinical trial. We will enroll patients with symptomatic neurogenic OH and randomize them to 1 of 2 treatments: (1) midodrine only, (2) atomoxetine only. We will follow up patients at 1 and 3 months after treatment. If the patients meet BP criteria for OH at 1 month, they will receive combination treatment with both midodrine and atomoxetin. The primary outcome measure is amelioration of questionnaire score evaluating OH-associated symptoms at 3 months. Secondary end-points were improvement in orthostatic blood pressure (BP) drop at 1 and 3 months.

Timeline

Start
2018-01-01
Primary completion
2019-01-29
Completion
2019-03-15

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Atomoxetine Other / unclassified 18 mg
Comparator Midodrine Small molecule 5 mg