Lung Cancer Registry for Lung Cancer Patients
LCR
Development of an Electronic Data Base for Lung Cancer Registry Which Will Include All the Epidemiological, Clinical, Pathological, Molecular and Treatment Parameters in Lung Cancer Patients Who Are Referred to a Tertiary Oncology Unit
1 other identifier
observational
650
1 country
1
Brief Summary
In the light of a new era in the management of lung cancer this non-interventional study intend to capture all the epidemiological, clinical, pathological, molecular and treatment parameters of non-small cell (NSCLC) and small cell (SCLC) lung cancer patients from a tertiary Oncology Clinic in an Electronic Data Base (EDB).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2017
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 8, 2017
CompletedFirst Submitted
Initial submission to the registry
August 23, 2017
CompletedFirst Posted
Study publicly available on registry
September 8, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 27, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
December 27, 2018
CompletedMarch 14, 2019
March 1, 2019
1.4 years
August 23, 2017
March 13, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Overall survival (OS)
Overall Survival (OS) will be recorded for all patients and it is defined as the time in months, from diagnosis till death by any cause.
12months
Secondary Outcomes (2)
Response Rate
12 months
Progression Free Survival
12 months
Study Arms (1)
Lung Cancer patients
All patients with lung cancer that referred to a tertiary Oncology Unit.
Eligibility Criteria
All patients with lung cancer that they have been referred to our Unit will be captured to this electronic database
You may qualify if:
- \- Since this will be a non-interventional study all adult patients who will be consent for registration of their data to EDB will be enrolled.
You may not qualify if:
- Patients with insufficient epidemiological or clinical data will be excluded such as patients with no demographic data or patients that have not taken at least 2 cycles of therapy.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
OCEBER
Athens, 11527, Greece
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Konstantinos N Syrigos, MD,PhD
Non-Governmental, Non-Profit Organization
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 23, 2017
First Posted
September 8, 2017
Study Start
August 8, 2017
Primary Completion
December 27, 2018
Study Completion
December 27, 2018
Last Updated
March 14, 2019
Record last verified: 2019-03