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A Prospective, Non-interventional Cohort Study of Subsolid Pulmonary Nodules

A Prospective, Non-interventional Cohort Study of Subsolid Pulmonary Nodules

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400093012
Enrollment
Unknown
Registered
2024-11-27
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Subsolid pulmonary nodules

Interventions

observation group:None

Sponsors

Guangdong Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age >=18 years old, gender unlimited; 2. The initial pulmonary nodule was >= 5 mm (including subsolid components) and <= 30 mm, and did not shrink or disappear after 3 months of follow-up; 3. ECOG 0 to 3; 4. Can provide DICOM format CT image data; 5. Sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Long-term use of immunosuppressants and hormone drugs; 2. Previous history of malignant tumors (if no recurrence or carcinoma in situ was found more than 5 years after radical treatment); 3. Can not cooperate with regular follow-up; 4. General condition is poor, life expectancy is less than 6 months.

Design outcomes

Primary

MeasureTime frame
5-year growth rate of subsolid pulmonary nodules;

Secondary

MeasureTime frame
Lung cancer specific 5-year survival rate;Median follow-up time for patients with solid pulmonary nodules until invasive diagnosis/intervention;The growth rate and imaging changes of different types of pulmonary nodules;Sensitivity ;specificity;

Countries

China

Contacts

Public ContactYang Xuening

Guangdong Provincial People's Hospital

yangxncn@qq.com+86 139 2271 3300

Outcome results

None listed

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