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CT Radiomics and Lung Ultrasound for Clinical Subtype Identification in Severe Pneumonia-Associated ARDS

CT Radiomics and Bedside Lung Ultrasound for Clinical Subtyping and Prognostic Impact of Fluid Management in Severe Pneumonia-Associated ARDS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500113099
Enrollment
Unknown
Registered
2025-11-25
Start date
2025-11-30
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Primary criteria for diagnosing severe pneumonia: 1) Requirement for invasive mechanical ventilation

Interventions

Severe pneumonia with ARDS group:None

Sponsors

Southern Medical University Southern Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Voluntarily sign an informed consent form; 2. Aged between 18 and 80 years; 3. Meet criteria for severe pneumonia with concomitant or progressive ARDS; 4. Projected ICU stay exceeding 48 hours.

Exclusion criteria

Exclusion criteria: 1.Unable to complete a single chest CT scan or LUS; 2.Has participated in other interventional studies; 3.Strict restriction of fluid intake is required, or explicit fluid resuscitation therapy is indicated. 4.Pregnant or breastfeeding women; 5.Contraindications for CT or ultrasound examinations; 6.The investigator has determined that the subject is unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
LUS pulmonary oedema-related data;

Secondary

MeasureTime frame
24-hour traffic volume;

Countries

China

Contacts

Public ContactZhenhua Zeng

Southern Medical University Southern Hospital

zhenhuazeng.2008@163.com+86 156 9242 8912

Outcome results

None listed

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