Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT05184829

A Single-center Study on the Effect of Systemic/Selective Lymph Node Dissection on the Prognosis of Ground Glass Nodules Smaller Than 3cm and With Components With Consolidation/Tumor Ratio Between 0.5-1

A single-center study on the effect of systemic/selective lymph node dissection on the prognosis of ground glass nodules smaller than 3cm and with components with consolidation/tumor ratio between 0.5-1

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

25 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

A single-center study on the effect of systemic/selective lymph node dissection on the prognosis of ground glass nodules smaller than 3cm and with components with consolidation/tumor ratio between 0.5-1

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Patients enrolled in the study must meet all of the following conditions:

  • 1.Aged between 25 and 75 years;
  • 2. GGO is diagnosed by thin-section lung CT (thickness <1.5mm) within one month before surgery;
  • 3. The maximum diameter of the GGO is smaller than 3cm;
  • 4. The solid component in GGO between 50%-100%;
  • 5. Preoperative examination showed that the patient could tolerate lobectomy;
  • 6. The patient is able to understand and comply with the study and has provided written informed consent.

Exclusion criteria

Patients meeting any of the following criteria are not eligible for this trial:

  • 1. Patients with a history of lung surgery;
  • 2. Postoperative pathology showed non-primary lung cancer;
  • 3. The scope of surgical resection is larger than one lung lobe;
  • 4. Patients with a history of other tumors;
  • 5. Patients with severe complications (coronary heart disease, valvular heart disease, end-stage renal disease, severe liver cirrhosis);
  • 6. Unable to cooperate with the researchers because of dementia or cognitive decline
  • 7. Other situations that are not in conformity with the standards and requirements of this trial.

Treatment and study plan

selective lymph node dissection

Other

selective lymph node dissection

Systemic Lymph Node Dissection

Other

Systemic Lymph Node Dissection

Primary outcomes

  1. Overall survival

    Time frame: From enrollment to 36 months after surgery

Secondary outcomes

  1. Complications

    Time frame: 1-2 Weeks after enrollment (after Surgery)

    The degrees of cough

Sponsors and collaborators

Lead sponsor

Shanghai Zhongshan Hospital

Other

Registry information

Important dates

Study start
2022
Primary completion
2028
Study completion
2029
First posted
Jan 11, 2022
Registry last updated
Jan 11, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.