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Trial · NCT04295993

Methylene Blue and Microcirculation in Septic Shock

NCT04295993, Phase 3, Unknown, Cairo University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Methylene Blue and Microcirculation in Septic Shock. Trials, record NCT04295993. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04295993

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Methylene Blue and Microcirculation in Septic Shock
NCT number
NCT04295993
Status
Unknown
Phases
Phase 3
Enrollment
32 participants, estimated
Lead sponsor
Cairo University
Conditions
Septic Shock
Interventions
Methylene Blue, Norepinephrine infusion
First posted
2020-03-05
Last updated
2020-03-05

Source ClinicalTrials.gov

Registered outcomes10

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryMicrovascular flow index6 hours
The image will be divided into four quadrants and the vessels \<20 μ m diameter will be assigned a score based on the predominant flow characteristics of the vessels in that quadrant (0 = absent flow; 1 = intermittent; 2 = sluggish; 3 = normal). The values in each quadrant will be averaged to give an microvascular flow index for each sublingual site at each time point. To determine heterogeneity of perfusion, the flow heterogeneity index will be calculated as the highest microvascular flow index minus the lowest microvascular flow index divided by the mean microvascular flow index.
SecondaryTotal vessel density6 hoursThe number of vessels per millimeters squared.
SecondaryPerfused vessel density6 hoursThe number of vessels multiplied by the fraction of perfused vessels
SecondaryProportion of perfused vessel6 hoursThe number of vessels with flows 2 and 3 divided by the total number of vessels and multiplied by 100.
Secondarymean arterial pressure24 hoursthe mean arterial blood pressure measured in mmHg
Secondaryserum lactate6 hoursthe value of lactate in the serum measured in milligrams per liter
Secondarylength of stay in the intensive care unit28 daysthe duration of stay in the intensive care unit measured in days
Secondarycardiac output24 hoursThe amount of blood ejected by the heart in one minute measured in liters
Secondarytotal consumption of norepinephrine6 hoursthe total consumption of norepinephrine in 6 hours measured in micrograms.
Secondaryincidence of mortality28 daysThe number of dead patients divided by the total number of patients

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT04295993

GET https://conductscience.org/api/trials/v1/NCT04295993/registered