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A Real-world Study to Explore Recurrence/Metastases of the NSCLC Patients and the Impact Factors of Patient Survivals

A Real-world Study to Explore Recurrence/Metastases of the Early-stage (I-IIIA) NSCLC Patients and the Impact Factors of Patient Survivals

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03710616
Enrollment
700
Registered
2018-10-18
Start date
2018-03-24
Completion date
2023-01-01
Last updated
2019-08-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-small Cell Lung Cancer

Keywords

early-stage NSCLC, real-world evidences, patient survivals

Brief summary

The real-world study was designed to explore recurrence/metastases of the patients with non-small cell lung cancer as measured by patient survivals and the impact factors of patient survivals.

Detailed description

The trial was designed as a real-world observational study to recruit those patients with pathologically diagnosed early-phase non-small cell lung cancer (NSCLC) who were enrolled in the clinical form 2009 to 2017 and explore recurrence/metastases of the NSCLC patients as measured by patient survivals and the impact factors of patient survivals. The study data on patient demographic characteristics, tumor biological characteristics, and clinicla treatments were collected via a retrospectively review method for evaluation of patient survivals and the relevance of clinical characteristics of the patients and patient survivals.

Interventions

PROCEDURESurgeries

Surgical operations plus systematic lymphadenectomies

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

The patients who meet all the following inclusion criteria will be included in the study: * The patients who were operated with radical operations of the lung cancer; * The patients with clinical I-IIIA staging tumors; * The pathologically diagnosed NSCLC patients;

Exclusion criteria

\- Not be specified;

Design outcomes

Primary

MeasureTime frameDescription
Disease-free survival rates within the configured observation periods2009-2017Disease-free survival rates within 3-month, 6-month, 1-year, 2-year, and 3-year observation periods;

Secondary

MeasureTime frameDescription
Disease-free survival rates at the configured locations and observation periods2009-2017Disease-free survival rates at the metastasized lymph nodes, bone, and brain within 3-month, 6-month, 1-year, 2-year, and 3-year observation periods;

Other

MeasureTime frameDescription
Impact factors of disease-free survival rates2009-2017Impact factors of disease-free survival rates
Overall rates2009-2017Overall rates within 3 month-, 6 month-, 1 year-, 2 year-, and 3 year- observation periods
Rates of perioperative complications2009-2017Rates of perioperative complications

Countries

China

Contacts

Primary ContactJianxing HE, MD
hejx@vip.163.com0086-20-83062114
Backup ContactWenhua LIANG, Ph.D
liangwh1987@163.com0086-20-83062114

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026