A Study to Evaluate Effectiveness of Sublobar Dissection in Patients With Non-small Cell Lung Cancer

NCT ID: NCT03427567

Last Updated: 2018-05-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

3902 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-12-01

Study Completion Date

2018-03-30

Brief Summary

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A study to evaluate effectiveness of sublobar dissection in patients with non-small cell lung cancer

Detailed Description

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This is a multi-centre real-world non-interventional observational study. The study data on patient demographic/tumor biological characteristics and clinical treatments were retrospectively collected to evaluate effectiveness of sublobar dissection in the Chinese patients with non-small cell lung cancer who received sublobar dissection.

Conditions

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Non-small Cell Lung Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Sublobar dissection

Chinese NSCLC patients who received sublobar dissection

Sublobar dissection

Intervention Type PROCEDURE

Sublobar dissection plus lymphadenectomy

Interventions

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Sublobar dissection

Sublobar dissection plus lymphadenectomy

Intervention Type PROCEDURE

Other Intervention Names

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Surgeries

Eligibility Criteria

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Inclusion Criteria

* Patients \>= 18 years old;
* Patients who received sublobar dissection from 2014 to 2017 (segment dissection/wedge dissection/segment and wedge dissections);
* Patients who received selective or systematic lymphadenectomy;
* Pathologically diagnosed patients with non-small cell lung cancer;
* Pathological staging: I, II

Exclusion Criteria

* Patients who received cancer treatments before surgeries (adjuvant therapies including chemotherapies, radiotherapies, target therapies);
* Patients who received late-phase or intolerant palliative lobectomy or compromise sublobar dissection;
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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LinkDoc Technology (Beijing) Co. Ltd.

INDUSTRY

Sponsor Role collaborator

Tongji Hospital

OTHER

Sponsor Role lead

Responsible Party

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XiangNing Fu

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Xiangning Fu, PhD

Role: PRINCIPAL_INVESTIGATOR

Tongji Hospital Affiliated to Tongji Medical College Huazhong Technology University

Locations

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China-Japan Friendship Hospital

Beijing, Beijing Municipality, China

Site Status

China PLA General Hospital

Beijing, Beijing Municipality, China

Site Status

Henan cancer hospital

Zhengzhou, Henan, China

Site Status

Tongji Hospital Affiliated to Huazhong Technology Hospital

Wuhan, Hubei, China

Site Status

Jiangsu cancer hospital

Nanjing, Jiangsu, China

Site Status

Xi'an Tangdu Hospital

Xi'an, Shaanxi, China

Site Status

Shanghai Chest Hospital

Shanghai, Shanghai Municipality, China

Site Status

Huaxi Hospital Affiliated to Sichuan University

Chengdu, Sichuan, China

Site Status

Tianjin Chest Hospital

Tianjin, Tianjin Municipality, China

Site Status

First Hospital Affiliated to Zhejiang University

Hangzhou, Zhejiang, China

Site Status

Countries

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China

Other Identifiers

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TJ-LC-01

Identifier Type: -

Identifier Source: org_study_id

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