Recruiting NCT06377592
Development and Accuracy Evaluation of Gram Staining Analysis AI
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Sample collection without intervention.
- Who it may be relevant to
- Registry conditions: Bacterial Infections. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Japan
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The investigators use Gram-stained specimens provided from clinical settings to develop and evaluate the accuracy of Gram staining analysis AI
Interventions
- Other Sample collection without intervention
No Intervention
Primary outcome measures
- Advanced level of blood culture Gram stain analysis AI accuracy [Time frame: Day1]
- Ordinary level of blood culture Gram stain analysis AI accuracy [Time frame: Day1]
Eligibility criteria
Inclusion criteria
- Patients in whom a Gram stain test was ordered
Exclusion criteria
- No exclusion criteria
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-only
Study locations
Japan · 1 center
- Osaka University Hospital — Suita
Identifiers
NCT: NCT06377592 · G22396