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Technical standard and application of intelligence assisted ultrasound indiagnosis of subpleural lung lesions

Technical standard and application of intelligence assisted ultrasound indiagnosis of subpleural lung lesions

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000029823
Enrollment
Unknown
Registered
2020-02-14
Start date
2020-04-01
Completion date
Unknown
Last updated
2020-02-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Subpleural pulmonary lesions

Interventions

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Sponsors

Shanghai Pulmonary Hospital affiliated to Tongji University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged between 16-80 years; 2. The lesion could be localized beneath the pleura by imaging examination; 3. The lesion was diagnosed by pathological, etiological examination or diagnostic therapy; 4. US images of the lesion were clear and could be preserved in whole; 5. Agree to participate in the trial and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. High risk of hypersensitivity to UCA; 2. Severe cardiovascular disease, liver or kidney dysfunction, mental disorders, etc.; 3. Other conditions that might affect the study.

Design outcomes

Primary

MeasureTime frame
Lesion morphology;Characteristics of color Doppler images;Elastic ultrasound score;Area under the TIC;Arrival intensity of lesion;Lesion-lung arrival time difference and chest wall-lesion arrival time difference;Imaging omics;

Secondary

MeasureTime frame
Characteristics of necrotic areas;Presence of vessel signs;Intensity at 60s, 120s and 180s;Proportion: the ratio of lesion-lung arrival time difference to chest wall-lung arrival time difference.;Peak intensity;Wash-in rate;Half intensity;Time from peak to half;

Countries

China

Contacts

Public ContactWang Yin

Shanghai Pulmonary Hospital affiliated to Tongji University

lpbbl@aliyun.com+86 13701885138

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026