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Trial · NCT06478797

Early Resuscitation in Paediatric Sepsis Using Inotropes

NCT06478797, Phase 2, Unknown, NATALIA LOPERA MUNERA

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Early Resuscitation in Paediatric Sepsis Using Inotropes. Trials, record NCT06478797. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06478797

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Trial

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

Title
Early Resuscitation in Paediatric Sepsis Using Inotropes
NCT number
NCT06478797
Status
Unknown
Phases
Phase 2
Enrollment
40 participants, estimated
Lead sponsor
NATALIA LOPERA MUNERA
Conditions
Sepsis
Interventions
Fluid, Adrenalin
First posted
2024-06-27
Last updated
2024-06-27

Source ClinicalTrials.gov

Registered outcomes19

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

ListOutcomeTime frameDescription
PrimarySurvival free of organ support at 28 daysFrom time of randomization until 28 days, if death occurs, time is set to 0 daysOrgan support will be defined as invasive ventilation support, cardiovascular organ support (inotropic or ECMO support), and renal replacement therapy
SecondaryRecuitment rates12 monthsSecondary feasibility outcome 1
SecondaryProportion of eligible randomised12 monthsOther feasibility 2
SecondaryProportion of eligible consented using perspective consent and consent to continue12 monthsOther feasibility 3
SecondaryTime to initiation of inotropes between the control and the early inotrope arm24 hoursOther feasibility 4
SecondaryAmount of fluid delivered (in mLs per kg) during the first 24 h between the control and the early inotrope arm24 hoursOther feasibility 5
SecondaryProtocol violations12 monthsOther feasibility 6. Percentage of patients not treated according to the assigned group.
SecondarySurvival free of inotrope support at 7 days7 daysSecondary exploratory clinical outcome 1
SecondarySurvival free of invasive ventilation support at 7 days7 daysSecondary exploratory clinical outcome 2
Secondary28-day mortalityFrom time of randomization until 28 daysSecondary exploratory clinical outcome 3

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.

Papers31

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
1335441BACKGROUNDPubMed
15636651BACKGROUNDPubMed
18427095BACKGROUNDPubMed
18829798BACKGROUNDPubMed
18929686BACKGROUNDPubMed
19325359BACKGROUNDPubMed
21615299BACKGROUNDPubMed
21768312BACKGROUNDPubMed
24862461BACKGROUNDPubMed
25471555BACKGROUNDPubMed

1 to 10 of 31

See all 31 papers

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/NCT06478797

GET https://conductscience.org/api/trials/v1/NCT06478797/papers?page=2