Methylene Blue as a Third-line Vasopressor in Septic Shock

Status Recruiting

Clinical Trial Summary

A randomized, prospective study comparing ProvayBlue® to standard care with multiple sympathomimetic vasopressors.

Clinical Trial Description

The study will be an un-blinded, Phase 2, randomized, 1:1, prospective trial comparing patients in septic shock receiving norepinephrine and vasopressin followed by phenylephrine versus ProvayBlue® as the third-line vasopressor. The third line vasopressor will be compared at 1 hour to see if it affects the patient's mean arterial blood pressure (MAP). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04089072
Study type	Interventional
Source	Carilion Clinic
Contact	Frank Biscardi, MD
Phone	540-981-7000
Email	fhbiscardi@carilionclinic.org
Status	Recruiting
Phase	Phase 2
Start date	December 1, 2019
Completion date	November 1, 2024

View Details

See also
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