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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01949181
Other study ID # 2010/37
Secondary ID
Status Completed
Phase N/A
First received September 19, 2013
Last updated May 2, 2016
Start date August 2011
Est. completion date March 2014

Study information

Verified date May 2016
Source Hopital Foch
Contact n/a
Is FDA regulated No
Health authority France: Agence Nationale de Sécurité du Médicament et des produits de santé
Study type Interventional

Clinical Trial Summary

Prospective research to study the relationship between concentrations of metals/metalloids in blood, hair and lung tissue with the occurence of lung cancer or chronic obstructive pulmonary disease.


Recruitment information / eligibility

Status Completed
Enrollment 251
Est. completion date March 2014
Est. primary completion date March 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Patients of 18 to 75 years of age.

- Patients admitted for lung resection (either cancerous or non-cancerous) or lung transplant

Exclusion Criteria:

- Patients with mental or physical conditions that prevent them giving their agreement for the study

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science


Intervention

Procedure:
Lung surgery


Locations

Country Name City State
France CHU de Poitiers, Chirurgie Cardiaque et Thoracique Poitiers
France Hopital Foch Suresnes Ile de France

Sponsors (1)

Lead Sponsor Collaborator
Hopital Foch

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Metals/metalloids concentration Blood, hair and lung tissue are sampled during lung surgery No
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