Interventional Ablation for Early-stage Lung Cancer

NCT07005999 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 656

Last updated 2025-06-05

No results posted yet for this study

Summary

What is this study about? This clinical trial aims to compare two treatments for high-risk lung nodules or early-stage lung cancer: interventional ablation (a minimally invasive procedure that destroys tumors with heat or cold) and surgical resection (surgery to remove the tumor). The goal is to determine if ablation is as safe and effective as surgery while preserving more lung function.

Why is this important? Lung cancer is a leading cause of cancer deaths worldwide. Early detection improves survival, but surgery can damage lung function.

Ablation (e.g., microwave, cryotherapy) is less invasive than surgery and may offer similar outcomes with faster recovery. However, more evidence is needed to confirm its role in early-stage disease.

Conditions

  • Lung Cancer (NSCLC)
  • Early Stage Lung Non-Small Cell Carcinoma

Sponsors & Collaborators

  • Hunan Provincial People's Hospital

    collaborator OTHER
  • Beijing Chao Yang Hospital

    collaborator OTHER
  • Fuda Cancer Hospital, Guangzhou

    collaborator OTHER
  • University of South China Affiliated Nanhua Hospital

    collaborator UNKNOWN
  • Nanfang Hospital, Southern Medical University

    collaborator OTHER
  • The First Affiliated Hospital of Guangzhou Medical University

    collaborator OTHER
  • Sir Run Run Shaw Hospital

    collaborator OTHER
  • Eastern Theater General Hospital,QinHuai District Medical Area

    collaborator UNKNOWN
  • The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

    collaborator OTHER
  • Emergency General Hospital

    collaborator OTHER
  • The First Affiliated Hospital of Anhui Medical University

    collaborator OTHER
  • The Second Hospital of Anhui Medical University

    collaborator OTHER
  • Huaxi Hospital

    collaborator OTHER
  • Shanghai Chest Hospital

    collaborator OTHER
  • Military 301 Hospital

    collaborator UNKNOWN
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    collaborator OTHER
  • Guangzhou Institute of Respiratory Disease

    lead OTHER

Principal Investigators

  • Chengzhi Zhou, Doctor · Guangzhou Institute of Respiratory Disease (Responsible Party)

Eligibility

Min Age
20 Years
Max Age
79 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-04-12
Primary Completion
2028-12-21
Completion
2028-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07005999 on ClinicalTrials.gov