Clinical trial · Observational
3D-US Construct on Volumetric Assessment of Lung Disease & Clinical Application
Three-dimensional Ultrasonic Construct on Volumetric Assessment of Lung Disease and Its Clinical Application
- 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)
The goal of this observational study is to establish the three-dimensional construct of lung lesion via ultrasound in patients with peripheral lung lesions or any superficial lesion in thoracic fields. The primary question our study aims to answer is: Whether the 3D ultrasound morphology can reflect lung disease entities? Whether the 3D volumetric follow-up protocol can be standardised to reflect lung disease status?
Conditions
Conditions (4)
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 (Diagnosis) | Malignant Lung Neoplasm | CURATED_EXACT | 0.85 |
| Lung Ultrasound | — | UNRESOLVED | — |
| Peripheral Lung Lesions | — | UNRESOLVED | — |
| Ultrasound Assessment | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
Design
Arms and outcomes
Arms (1)
- label
- ultrasound work-up
- description
- participants with peripheral lesions, not confined to lung, referred for ultrasound workup
Primary outcomes (1)
- measure
- volume of measured lesion
- timeFrame
- from enrollment, every 6 weeks until 24th week
- description
- Standard volume will be defined by computed tomography measurement, and the ultrasound 3D-volmetric result would be compared
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Participants suspect with lung lesions referred for ultrasound workup Exclusion Criteria: * Participants aged \< 18 years * Participants refusal * Participants with implanted metal in scanning area interfering data collection * Participants who cannot perform breath holding for at least 1 second
References
Publications (0)
Data not yet available