Clinical trial · Interventional
Feasibility of Multi-Energy Digital Radiography Detector for Lung Lesions Detection
Feasibility of Single Exposure Dual Energy Subtraction With a Multi-Energy Digital Radiography Detector for Lung Lesions Detection
NCT03528733CI-TRIAL-00042684unknownN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
A single-centre, industry sponsored, pilot study to assess the feasibility of Single Exposure Dual Energy Subtraction with a Multi-Energy digital radiography detector as an imaging platform for lung lesion detection.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Lung Tumor | Lung Neoplasm | ALIAS | 0.90 |
| Solitary Pulmonary Nodule | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Multi-Energy Digital Radiography Detector System | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Multi-Energy Detector
- description
- Multi-Energy Digital Radiography Detector System
- interventionNames
- Device: Multi-Energy Digital Radiography Detector System
Primary outcomes (1)
- measure
- Multi-Energy images will be compared to baseline Chest CT images for visualizing lung lesions.
- timeFrame
- 3 months
- description
- Multi-Energy images will be compared to baseline Chest CT images for visualizing lung lesions, as determined. Expert readers will qualitatively evaluate the imaging differences (e.g. motion artifacts, technical defects, ease of anomalies identification, etc) with an evaluation form with a questionnaire grading system (i.e. 1 (severe defect), 2 (moderate defect) to 5 (no defect)).
Secondary outcomes (1)
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Age 18 years and older. * Patients with previously diagnosed carcinoma with lung metastases, or patients with previously detected lung nodule * Subject is able to provide informed consent * Study participant is scheduled to have a chest CT exam as part of their routine care. * Study participant is able to stand and be still during the exams. Exclusion Criteria: * Not able or willing to provide Informed Consent, or consent is withdrawn. * Study participant is pregnant * Study participant is unable to perform standard radiography exam and CT exam
References
Publications (0)
Data not yet available
No reference posted for this study.