A Dose Titration of Droxidopa in Patients With Spinal Cord Injury

Completed · Phase 1 · Has a placebo group

Conditions studied: Spinal Cord Injury, Hypotension

In brief

The investigators seek to determine the efficacy, duration of action and safety of escalating dose of droxidopa on systemic blood pressure, cerebral blood flow and vasoactive hormones and catecholamines during upright seated posture. Primary Question: 1\. What is the lowest dose of droxidopa that increases seated SBP to 115±5 mmHg in men and 105±5 mmHg in women? * When does the defined increase in SBP occur after oral ingestion of droxidopa? * How long does this dose of droxidopa sustain SBP at these levels? * What are the vital signs and the subjective symptomology following droxidopa administration? Secondary Question: 1\. What is the MFV response to droxidopa administration in hypotensive individuals with SCI? * Does an increase in SBP correspond to an increase in MCA MFV? Tertiary Question: 1\. What is the vasoactive hormone and catecholamine response to droxidopa administration in hypotensive individuals with SCI? * Does droxidopa administration result in a change in APR, Aldo or NE in hypotensive individuals with SCI?

Key facts

Study ID
NCT01354158
Run by
Bronx VA Medical Center
People needed
11
Starts
2011-05-01
Expected to finish
2013-05-01
Last updated by the study team
2013-07-30

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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