Clinical trial · Interventional
EPIONE Guided Lung Evaluation
Prospective Clinical Investigation on the Evaluation of Performance and Safety of the EPIONE Assisted CT-guided Percutaneous Procedures in the Lungs
NCT05651867CI-TRIAL-00092119EGLEcompletedN/AResults postedClinicalTrials.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)
Interventional clinical study to obtain performance and safety data of the EPIONE® device when used for percutaneous procedures in the lung.
Conditions
Conditions (1)
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 Cancer | Malignant Lung Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| EPIONE device | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Interventional arm
- description
- Patients treated by percutaneous CT-guided procedures in the lung with the EPIONE® device
- interventionNames
- Device: EPIONE device
Primary outcomes (1)
- measure
- Feasibility of the Device
- timeFrame
- an average of 7 months
- description
- Number of lesion target reached ; the lesion target is considered reached when the needle is positioned accurately enough as compared to the planning to allow the planned procedure to be performed.
Secondary outcomes (6)
- measure
- Needle Placement Accuracy
- timeFrame
- an average of 7 months
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patient ≥18 years old, * Patient for whom a percutaneous CT-guided intervention in lung has been prescribed and agreed by a multidisciplinary team of radiologists, surgeons and clinicians, * Patient with a signed informed consent form. * Patient covered by a social security system. Exclusion Criteria: * Patient unable to undergo general anesthesia, * Pregnant or nursing female, confirmed before the intervention * Patient already participating in another clinical study
References
Publications (0)
Data not yet available
No reference posted for this study.