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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

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Fudan University

Status

Not yet enrolling

Conditions

Postoperative Recovery
Progression

Treatments

Other: selective lymph node dissection
Other: Systemic Lymph Node Dissection

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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

Full description

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

Enrollment

500 estimated patients

Sex

All

Ages

25 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

  • 1.Aged between 25 and 75 years;
    1. GGO is diagnosed by thin-section lung CT (thickness <1.5mm) within one month before surgery;
    1. The maximum diameter of the GGO is smaller than 3cm;
    1. The solid component in GGO between 50%-100%;
    1. Preoperative examination showed that the patient could tolerate lobectomy;
    1. 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;
    1. Postoperative pathology showed non-primary lung cancer;
    1. The scope of surgical resection is larger than one lung lobe;
    1. Patients with a history of other tumors;
    1. Patients with severe complications (coronary heart disease, valvular heart disease, end-stage renal disease, severe liver cirrhosis);
    1. Unable to cooperate with the researchers because of dementia or cognitive decline
    1. Other situations that are not in conformity with the standards and requirements of this trial.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

500 participants in 2 patient groups

systemic lymph node dissection group
Active Comparator group
Description:
systemic lymph node dissection group
Treatment:
Other: Systemic Lymph Node Dissection
selective lymph node dissection
Experimental group
Description:
selective lymph node dissection
Treatment:
Other: selective lymph node dissection

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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