Ultrasound Findings in a Pediatric Population
NCT07919613, Not yet recruiting, Odense University Hospital
Trial 8
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Ultrasound Findings in a Pediatric Population | ClinicalTrials.gov |
| NCT number | NCT07919613 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Enrollment | 138 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Odense University Hospital | ClinicalTrials.gov |
| Conditions | Respiratory Tract Infections (RTI), Lung Ultrasound | ClinicalTrials.gov |
| First posted | 2026-11-05 | ClinicalTrials.gov |
| Last updated | 2026-11-05 | ClinicalTrials.gov |
Registered outcomes 9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Focused Thoracic ultrasound findings in a children admitted to a pediatric emergency department, divided into type | FTUS should be performed within the first 4-hours of admission to the pediatric emergency department | Type of ultrasound findings relevant: Lungsliding present? yes/no Lungpulse present? yes/no B-lines present? yes/no Consolidation present? yes/no Subpleural consolidation present? yes/no Pleural effusion present? yes/no Pleural thickness og irregulations? yes/no | ClinicalTrials.gov |
| Primary | Characterization of findings on Focused Thoracic ultrasound, in a children admitted to a pediatric emergency department | FTUS should be performed within the first 4-hours of admission to the pediatric emergency department | Characterization: Number of B-lines in zones with B-lines present Size of consolidations in mm Size of subpleural consolidations in mm Pleural effusion - simple or complex Thickness of pleura if thickened | ClinicalTrials.gov |
| Secondary | Proportion of children who undergo examination of all 14-zones | FTUS should be performed within the first 4-hours of admission to the pediatric emergency department, and data regarding number of examined zones will be noted in RedCap database within the following hour of FTUS examination | Number of children who undergo examination of 14-zones | ClinicalTrials.gov |
| Secondary | Time to complete examination | FTUS should be performed within the first 4-hours of admission to the pediatric emergency department, and data regarding the time spend on the examination will be noted within the first hour following the FTUS examination | How many minutes it takes to complete the examination | ClinicalTrials.gov |
| Secondary | Type of transducer used for examination | FTUS should be performed within the first 4-hours of admission to the pediatric emergency department, and data regarding the type of transducer and preset used, will be noted in our RedCap datase within the following hour of FTUS examination | Number of zones scanned using a linear transducer, and number of zones scanned using convex transducer | ClinicalTrials.gov |
| Secondary | Type of transducer-preset used for examination | FTUS should be performed within the first 4-hours of admission to the pediatric emergency department, and data regarding the type of transducer and preset used, will be noted in our RedCap datase within the following hour of FTUS examination | Number of zones scanned using a lung-preset, and number of zones scanned using abdominal-preset | ClinicalTrials.gov |
| Secondary | Quality of images on a Likert-scale of 1-3 and interrater reliability | Children admitted to a pediatric emergency department between 1 of October 2026 and 1 of May 2027 | 1. Not usefull: Images of insufficient quality for diagnostic purposes; key structures not identifiable. 2. Useful but not optimal for diagnostic imaging: Images of adequate quality to support interpretation, but with limitations such as suboptimal gain, depth, or partial obscuration. 3. Useful and optimal for diagnostic imaging: High-quality images with clear anatomical landmarks and artifact patterns sufficient for confident interpretation | ClinicalTrials.gov |
| Secondary | The childs position during the scan | FTUS should be performed within the first 4-hours of admission to the pediatric emergency department, and data regarding the position of the child, will be noted in our RedCap datase within the following hour of FTUS examination | Is the child sitting og lying during the scan | ClinicalTrials.gov |
| Secondary | Association between focused thoracic ultrasound findings and final diagnosis | 5-7 days after the child has been discharged, the final diagnosis will be extracted from their medical journal and put into our RedCap database. This allows sufficient time for the results of microbiological testing to be completed and registered | The association between focused thoracic ultrasound findings and the final clinical diagnosis established during the hospital admission.This includes assessing whether specific ultrasound findings or combinations of findings are associated with particular diagnoses | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)