drugset / Trial / NCT06133075

Using Mirabegron to Increase BP in Patients With POTS

NCT06133075

Phase 2 Completed 20 enrolled Cedars-Sinai Medical Center
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a pilot dose-finding study to test the hypothesis that mirabegron increases systolic blood pressure (BP), prevents syncope/presyncope, and improves the quality of life (QOL), functional capacity, chest pain, and overactive bladder (OAB) symptoms in patients with postural orthostatic tachycardia syndrome (POTS) who have a documented history of hypotension inadequately responsive to conventional treatments. The American Heart Association funds this study.

Timeline

Start
2023-12-22
Primary completion
2025-05-20
Completion
2025-07-25

Drugs

EvaluationDrugModalityDoseRoute
Comparator Mirabegron Other / unclassified 25 mg
Comparator Mirabegron Other / unclassified 50 mg