MedPath

Tunisian Lung Cancer Study

Recruiting
Conditions
Pulmonary Cancer
Registration Number
NCT06934499
Lead Sponsor
Dacima Consulting
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
1334
Inclusion Criteria
  • 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
Exclusion Criteria
  • None

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Diagnostic delayDay 1

Delay to set the pulmonary cancer diagnosis

Survival12 months

Overall survival

Relapse12 months

Time to relapse

Secondary Outcome Measures
NameTimeMethod
Recommendation ComplianceDay 1

Compliance to national and international guidance of pulmonary cancer management

Trial Locations

Locations (2)

Tunisian Society of Medical Oncology

🇹🇳

Ariana, Tunisia

Tunisian Society of Respiratory Diseases and Allergology

🇹🇳

Tunis, Tunisia

Tunisian Society of Medical Oncology
🇹🇳Ariana, Tunisia
Soraya Fenniche, MD
Contact
+216 98 586 490
soraya.fenniche@yahoo.fr
Nesrine Mejri, MD
Contact
97 429 933
nesrinemejriturki2@gmail.com

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.