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NCT04527419Recruiting

SLND or Not in cT1 GGO Invasive Lung Adenocarcinoma (ECTOP-1009)

Systematically Mediastinal Lymph Node Dissection or Not in Stage T1 Ground-glass Dominated Invasive Lung Adenocarcinoma: a Multi-center, Prospective Clinical Trial

Source: ClinicalTrials.gov · Last updated 26 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a study from Eastern Cooperative Thoracic Oncology Project, numbered as ECTOP-1009. Systematically mediastinal lymph node dissection or not in clinical stage T1 ground-glass dominated invasive lung adenocarcinoma: a multi-center, prospective clinical trial

Status (registry)
Recruiting
Study type
Interventional
Enrollment
545 (estimated)
First submitted
23 Aug 2020
Start date
9 Feb 2022
Primary completion date
21 Jul 2026
Lead sponsor
Fudan University
Diseases
Lung cancer
NCT number
NCT04527419

What you commit to

  • Study type: Interventional
  • Planned participants: 545
  • From 9 Feb 2022 to the primary completion date, 21 Jul 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who have received radiation, chemotherapy or other treatments previously.

Other illness

  • Patients undergoing wedge resection but not meeting the specific conditions of a Consolidation/Tumor Ratio (CTR) ≤ 0.25 AND a maximum tumor diameter ≤ 2 cm, based on the oncological outcomes of the JCOG0804/WJOG4507L trial.
  • Patients who have history of other malignant tumors.
  • Patients who have history of thoracic surgery.

Other

  • Other than invasive adenocarcinoma by pathological analysis.
  • Not complete resected or curative intent.

Who the study is looking for

  • Clinical stage T1N0M0 and planned curative surgery.
  • A single lesion detected on computed tomography (CT) scan featured as ground glass nodule(GGO) and C/T ratio ≤0.5.
  • Age 18 to 75.
  • Patients who have signed the informed consent form.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Fudan University Shanghai Cancer Center
Coordinator of this site? Confirm its status
ShanghaiChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.