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NCT04970602

The Effect of Early Use of Methylene Blue on Hemodynamics in Septic Shock

Status unknown NA Last updated 21 July 2021
What this trial tests

NA trial testing Methylene Blue in Septic Shock in 106 participants. Status unknown.

Timeline
20 June 2021
Primary endpoint
30 June 2023
1 January 2024

Quick facts

Lead sponsorXiangya Hospital of Central South University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment106
Start date20 June 2021
Primary completion30 June 2023
Estimated completion1 January 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Xiangya Hospital of Central South University

Who can join

18 and older, any sex, with Septic Shock. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will include patients requiring high dose of norepinephrine (NA) to maintain blood pressure after fluid resuscitation. The patients will be randomized into two groups, the study protocol is early combined application of methylene blue. The primary outcome is Sequential Organ Failure Assessment (SOFA) score 72 hours after admission. Second outcome includes duration of shock, length of intensive care unit (ICU) hospitalization and so on. To explore the underlying mechanism, the changes of sublingual microcirculation before and after vasopressor combination will be collected, also is the global longitudinal strain of left ventricle.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Methylene Blue

Trials testing the same drug.

Other recruiting trials for Septic Shock

Currently open trials in the same condition.

Other Xiangya Hospital of Central South University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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