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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06031181
Other study ID # SAFROS
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date March 31, 2023
Est. completion date December 31, 2030

Study information

Verified date December 2023
Source Fudan University
Contact Chaoqiang Deng
Phone +86-13122677592
Email fdudengcq@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a clinical trial from Eastern Cooperative Thoracic Oncology Project (ECTOP), numbered as ECTOP-1019. The goal of this clinical trial is to confirm the therapeutic effect of sublobar resection for AIS/MIA diagnosed by intraoperative frozen section.


Recruitment information / eligibility

Status Recruiting
Enrollment 390
Est. completion date December 31, 2030
Est. primary completion date January 1, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: 1. Patients who sign the informed consent form and are willing to complete the study according to the plan; 2. Aged from 18 to 80 years old; 3. ECOG equals 0 or 1; 4. Not receiving lung cancer surgery before; 5. Resectable peripheral cT1N0M0 tumors; 6. Single lung nodules with ground-glass dominant or pure ground-glass on CT, or multiple lung nodules with the major lesion being the aforementioned nodules; 7. Adenocarcinoma in Situ/Minimally Invasive Adenocarcinoma Diagnosed by Intraoperative Frozen Section 8. Not receiving chemotherapy or radiotherapy before. Exclusion Criteria: 1. Not cT1N0M0; 2. Cannot be completely resected by sublobar resection; 3. Invasive lung adenocarcinoma or not lung adenocarcinoma diagnosed cytologically or pathologically; 4. Receiving lung cancer surgery before; 5. Receiving radiotherapy or chemotherapy.

Study Design


Intervention

Procedure:
Sublobar Resection
Sublobar Resection includes segmentectomy and wedge resection

Locations

Country Name City State
China Fudan University Cancer Center Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Fudan University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary 5-year recurrence-free survival The event is defined as the tumor recurrence. 5 years
Secondary 5-year overall survival The event is defined as the death due to any causes. 5 years
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