A Study to Evaluate Effectiveness of Sublobar Dissection in Patients With Non-small Cell Lung Cancer
A Multi-centre Real-world Non-interventional Observational Study to Evaluate Effectiveness of Sublobar Dissection in the Chinese Patients With Non-small Cell Lung Cancer
1 other identifier
observational
3,902
1 country
10
Brief Summary
A study to evaluate effectiveness of sublobar dissection in patients with non-small cell lung cancer
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2017
Shorter than P25 for all trials
10 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2017
CompletedFirst Submitted
Initial submission to the registry
February 2, 2018
CompletedFirst Posted
Study publicly available on registry
February 9, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
March 30, 2018
CompletedMay 21, 2018
May 1, 2018
Same day
February 2, 2018
May 18, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Overall survival
Overall survival
2014 - 2017
Secondary Outcomes (1)
Overall survivals in subgroups
2014 - 2017
Other Outcomes (4)
Impact factors of overall survival
2014 - 2017
Death rates after surgeries
2014 - 2017
Impact factors of death rates after surgeries
2014 - 2017
- +1 more other outcomes
Study Arms (1)
Sublobar dissection
Chinese NSCLC patients who received sublobar dissection
Interventions
Sublobar dissection plus lymphadenectomy
Eligibility Criteria
Chinese patients with pathological diagnosed non-small cell lung cancer who received sublobar dissection and lymphadenectomy
You may qualify if:
- 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
You may not qualify if:
- 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;
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Tongji Hospitallead
- LinkDoc Technology (Beijing) Co. Ltd.collaborator
Study Sites (10)
China-Japan Friendship Hospital
Beijing, Beijing Municipality, 100029, China
China PLA General Hospital
Beijing, Beijing Municipality, 100853, China
Henan cancer hospital
Zhengzhou, Henan, 450003, China
Tongji Hospital Affiliated to Huazhong Technology Hospital
Wuhan, Hubei, 430030, China
Jiangsu cancer hospital
Nanjing, Jiangsu, 210009, China
Xi'an Tangdu Hospital
Xi'an, Shaanxi, 710000, China
Shanghai Chest Hospital
Shanghai, Shanghai Municipality, 200030, China
Huaxi Hospital Affiliated to Sichuan University
Chengdu, Sichuan, 610041, China
Tianjin Chest Hospital
Tianjin, Tianjin Municipality, 300051, China
First Hospital Affiliated to Zhejiang University
Hangzhou, Zhejiang, 310003, China
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Xiangning Fu, PhD
Tongji Hospital Affiliated to Tongji Medical College Huazhong Technology University
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
February 2, 2018
First Posted
February 9, 2018
Study Start
December 1, 2017
Primary Completion
December 1, 2017
Study Completion
March 30, 2018
Last Updated
May 21, 2018
Record last verified: 2018-05
Data Sharing
- IPD Sharing
- Will not share