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Epidemiological Study to Describe Non Small Cell Lung Cancer Clinical Management Patterns in MENA. Lung-EPICLIN/ Gulf

Epidemiological Study to Describe NSCLC Clinical Management Patterns in MENA

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01562665
Acronym
Lung-EPICLIN/G
Enrollment
25
Registered
2012-03-26
Start date
2012-06-30
Completion date
2015-02-28
Last updated
2016-05-24

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

Conditions

Non Small Cells Lung Cancer

Keywords

All patients with NSCLC attending participating hospitals

Brief summary

The overall aim of the study is: To provide accurate and reliable information regarding NSCLC clinical management across MENA region in order to detect unmet medical needs of this disease in terms of: * Patient and hospital characteristics. * Diagnostic and treatment approaches: initial and subsequent. * Follow-up patterns in clinical management. * Outcomes: symptoms, death, functionality, quality of life. * Use of resources and burden on patients and health care systems.

Detailed description

Epidemiological study to describe NSCLC clinical management patterns in MENA

Interventions

None listed

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Confirmed NSCLC diagnosis (e.g. bronchoscope or FNAB), all stages, men and women, attending the responsible department of treating this type of patients for the first time between November 1st, 2011 and August 30th, 2012 For PRO * Sub-sample: * ability to read and write since they will be asked to participate in the PRO part of the study. * Selection will not be based on the disease stage of each patient, in order to avoid a selection bias.

Exclusion criteria

* According to the study design there will not be any

Design outcomes

Primary

MeasureTime frame
Use of health resources by collecting data about hospital description and characteristics, Disease Diagnosis Procedures and Therapy informationApril 2014(26 Months)

Secondary

MeasureTime frame
Patient-Reported Outcomes (PRO) through self-administered questionnaires and the patients will be asked to complete them at each evaluation visit(25% of the whole sample)April 2014(26 Months)

Countries

Bahrain, Qatar, United Arab Emirates

Outcome results

None listed

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