About this trial
This is a prospective, multicenter, observational, national study. Eligible patients will be recruited consecutively among subjects with proven lung cancer, including any disease stage withclinical, therapeutic and evolutive discription.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age more than 18 years
Patients receiving health care in the departments of pulmonology, oncology, radiation oncology and thoracic surgery, whose diagnosis is confirmed histologically and/or by cytology, at least 3 months before the inclusion date
Informed consent
Disqualifiers
None
Trial population
All participants diagnosed with histologically confirmed lung cancer will be included in the study, regardless of sex, age, stage and histological subtype. Patients will be enrolled in the study consecutively The study will be conducted in different regions of Tunisia, encompassing several sites covering different departments in public hospitals.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Diagnostic delay
Delay to set the pulmonary cancer diagnosis
Survival
Overall survival
Relapse
Time to relapse
Secondary outcomes
Recommendation Compliance
Compliance to national and international guidance of pulmonary cancer management
Other outcomes
Multidisciplinary Consultation Meetings
Number of Multidisciplinary Consultation Meetings
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Dacima Consulting
Lead sponsor
The Multidisciplinary Consultation Meeting Thoracic Oncology of the Abderrahmen Mami Hospital (ROTHAM)
Collaborator
Tunisian Society of Respiratory Diseases and Allergology
Collaborator
Tunisian Society of Medical Oncology
Collaborator