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Not yet recruiting NCT07574255

3D-US Construct on Volumetric Assessment of Lung Disease & Clinical Application

— Observational Lung Ultrasound Lung Cancer (Diagnosis) Peripheral Lung Lesions Ultrasound Assessment

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
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Lung Ultrasound, Lung Cancer (Diagnosis), Peripheral Lung Lesions, Ultrasound Assessment. Basic parameters: from 18 years · 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
Taiwan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Three-dimensional Ultrasonic Construct on Volumetric Assessment of Lung Disease and Its Clinical Application

Overview

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?

Primary outcome measures

  • volume of measured lesion [Time frame: from enrollment, every 6 weeks until 24th week]

Eligibility criteria

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

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
Cohort

Study locations

Taiwan · 1 center
  • National Taiwan University Hospital — Taipei

Identifiers

NCT: NCT07574255 · 202604005DIND

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗