Management of Advanced Non-Small Cell Lung Cancer (NSCLC) and Clinical Outcomes in Patients Who Received Gefitinib in Thailand

NCT ID: NCT01130961

Last Updated: 2010-10-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

104 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-10-31

Study Completion Date

2010-08-31

Brief Summary

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The purpose of this study is to determine progression-free survival of lung cancer patients who received gefitinib in clinical practice in Thailand.

Detailed Description

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Conditions

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Lung Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Diagnosed as having lung cancer based on histological/cytological findings
* Admitted to the hospital between January 2004 and December 2008
* Treated with gefitinib for at least 3 months

Exclusion Criteria

* Involvement in the planning and/or conduct of the study
* Participation in another clinical study during the last 3 months
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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AstraZeneca

INDUSTRY

Sponsor Role lead

Responsible Party

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AstraZeneca

Principal Investigators

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Virote Sriuranpong, MD., PhD.

Role: PRINCIPAL_INVESTIGATOR

Chulalongkorn Hospital, Bangkok, Thailand

Vichien Srimuninnimit, MD.

Role: PRINCIPAL_INVESTIGATOR

Siriraj Hospital, Bangkok, Thailand

Locations

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Research Site

Bangkok, , Thailand

Site Status

Countries

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Thailand

Other Identifiers

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NIS-OTH-IRE-2009/1

Identifier Type: -

Identifier Source: org_study_id