drugset / Trial / NCT02553265

Carbidopa for the Treatment of Excessive Blood Pressure Variability

NCT02553265

Phase 2 Completed 22 enrolled NYU Langone Health
RandomizedCrossoverQuadruple-blindTreatment

Summary

The overall study objectives are to determine whether carbidopa (Lodosyn®) is safe and well tolerated and to assess whether it can inhibit catecholamine-induced paroxysmal hypertension and normalize or reduce the exaggerated blood pressure variability in patients with familial dysautonomia (FD, also called hereditary sensory and autonomic neuropathy type III or Riley-Day syndrome). Funding Source- FDA OOPD.

Timeline

Start
2015-09
Primary completion
2019-05-10
Completion
2019-05-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Carbidopa Unknown 300 mg
Subject Carbidopa Unknown 600 mg