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Trial · NCT07085624

Early Optimization of Ceftazidime Regimen in Critical Care

NCT07085624, Not applicable, Not yet recruiting, Centre Hospitalier Universitaire de Saint Etienne

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Early Optimization of Ceftazidime Regimen in Critical Care. Trials, record NCT07085624. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07085624

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Trial

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

Title
Early Optimization of Ceftazidime Regimen in Critical Care
NCT number
NCT07085624
Status
Not yet recruiting
Phases
Not applicable
Enrollment
128 participants, estimated
Lead sponsor
Centre Hospitalier Universitaire de Saint Etienne
Conditions
Infection in ICU, Sepsis, Septic Shock, Pseudomonas Aeruginosa Infection
Interventions
ceftazidime, plasma ceftazidime dosage
First posted
2025-07-25
Last updated
2026-09-16

Source ClinicalTrials.gov

Registered outcomes7

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

ListOutcomeTime frameDescription
Primary
Percentage of subjects with a ceftazidime concentration equal to or above the target concentration threshold (35 mg/L) at both 3h and 24h after the first administration, and below the toxicity threshold of 100 mg/L.
24 hours
SecondaryPatient severity assessed using the SOFA (Sequential Organ Failure Assessment Score)day 7SOFA score from 0 to 24 The higher the score (24), the greater the incidence of organ failure
Secondarydeathday 28
SecondaryOccurrence of neurological adverse events defined as: seizure, myoclonus, encephalopathy or delirium, altered consciousness (Glasgow score)day 28
SecondaryOccurrence of an overdose defined as a concentration greater than 100 mg/L.day 28
SecondaryRenal function assessmentday 28creatinine clearance (mL/mn) with the CKD-EPI (Chronic Kidney Disease - Epidemiology Collaboration) equation
SecondaryTime to reach PK/PD (pharmacokinetics/pharmacodynamics) targets24 hours

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/NCT07085624

GET https://conductscience.org/api/trials/v1/NCT07085624/registered