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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00213798
Other study ID # 2731
Secondary ID
Status Completed
Phase N/A
First received September 13, 2005
Last updated August 29, 2011
Start date December 2003
Est. completion date August 2011

Study information

Verified date August 2011
Source University Hospital, Strasbourg, France
Contact n/a
Is FDA regulated No
Health authority France: Ministry of Health
Study type Interventional

Clinical Trial Summary

The majority of lung cancer patients have a tumor-derived genetic alteration in circulating plasma DNA that could be exploited as a diagnostic tool. The aim of this study is to evaluate if plasma DNA can be used as a valuable non invasive test to monitor disease progression without assessing the tumor.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date August 2011
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Presence of lung tumor to use fiberoscopy or surgical intervention for diagnosis.

- No lung instability.

- Individuals give all informed consent

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Screening


Intervention

Procedure:
Biopsy samples


Locations

Country Name City State
France Service de Chirurgie Thoracique, Hôpital Civil Strasbourg
France Service de Pneumologie, Hôpital Civil Strasbourg
France Service de Pneumologie, Hôpital de Hautepierre Strasbourg
France Service de Pneumologie, Hôpital Lyautey Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

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