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Identifying Local Signs at the Catheter Insertion Site With Artificial Intelligence

Development of an Artificial Intelligence Model of Image Recognition Through Images of Intravascular Catheters From Inpatients and Outpatients to Identify the Presence of Local Signs Associated With Infection

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05440396
Acronym
DeepCath
Enrollment
1000
Registered
2022-06-30
Start date
2022-09-01
Completion date
2023-12-31
Last updated
2022-10-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Catheter Infection

Keywords

catheter infection, deep learning, local signs

Brief summary

Deepcath is the first step to the introduction of artificial intelligence in catheter care. A better use of visualisation of catheter exit site should be used not only by the HCWs but also by the patients and their family. A deep learning system able to detect visual abnormalities of the catheter exit site will be an helpful tools to develop a continuous follow-up of intravascular catheters.

Interventions

DIAGNOSTIC_TESTPhotographs collection phase

Three medical experts have been selected to review the photo collected. Each expert medical assesses the presence of local signs of infection on the photographs by annotating them directly via a dedicated software. They will annotate local signs: redness, perfusion extravasation, necrosis, hematoma, edema, non-purulent discharge, and purulent discharge. A convolutional neural network model will determine the probability of local sign presence. Each picture will be annotated to determine the main characteristics of the catheter. A dataset preparation with photo cropping will be performed for modelling.

Sponsors

Assistance Publique - Hôpitaux de Paris
CollaboratorOTHER
National Network Surveillance and Prevention of Infections Associated with Invasive Devices SPIADI
CollaboratorUNKNOWN
University Hospital, Clermont-Ferrand
CollaboratorOTHER
University Hospital, Grenoble
CollaboratorOTHER
UNICANCER
CollaboratorOTHER
University Grenoble Alps
CollaboratorOTHER
Outcome Rea
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients over 18 years of age Patients with one or more implanted central venous, midline, piCCline, arterial, or peripheral catheters. Patient and/or trusted person and/or family who have verbally stated their non-objection to the study Patient affiliated or beneficiary of a social security plan

Exclusion criteria

Patients presenting a peripheral identification sign close to the catheter insertion point cannot be masked when the photograph is taken. Thus, jewelry, clothing, tattoos, scars, and birthmarks are identifying features. Patients whose catheter insertion point is not visible.

Design outcomes

Primary

MeasureTime frameDescription
The number of correct predictions for redness divided by the total number of predictionsthrough study completion, an average of 1 yearOverall classification accuracy of the learning model compared to the assessment of three independent medical experts on the detection of the presence of redness greater than or equal to 5 mm at the catheter insertion site.

Secondary

MeasureTime frameDescription
The ratio of true positives and total positives predicted:through study completion, an average of 1 yearThe precision metric focuses on Type-I errors(FP). A Type-I error occurs when we reject a true null Hypothesis.
The number of correct predictions for indurated venous cord divided by the total number of predictionsthrough study completion, an average of 1 yearEvaluate, on the basis of images of peripheral catheter insertion sites, the reliability of the learning model on the assessment of the presence of indurated venous cord.
The link between presence of local signs and infectionthrough study completion, an average of 1 yearMeasure the correlation between the appearance of the catheter puncture site and the presence of signs consistent with local and systemic infection.

Countries

France

Contacts

Primary ContactJean-François TIMSIT, Pr
jean-francois.timsit@aphp.fr+33140257703

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026