NCT01949181

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
251

participants targeted

Target at P75+ for not_applicable lung-cancer

Timeline
Completed

Started Aug 2011

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2011

Completed
2.1 years until next milestone

First Submitted

Initial submission to the registry

September 19, 2013

Completed
5 days until next milestone

First Posted

Study publicly available on registry

September 24, 2013

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2014

Completed
Last Updated

May 3, 2016

Status Verified

May 1, 2016

Enrollment Period

2.6 years

First QC Date

September 19, 2013

Last Update Submit

May 2, 2016

Conditions

Keywords

MetalsMetalloidsBloodHairLungLung cancerChronic obstructive pulmonary disease

Outcome Measures

Primary Outcomes (1)

  • Metals/metalloids concentration

    Blood, hair and lung tissue are sampled during lung surgery

Study Arms (1)

Pulmonary cancer

EXPERIMENTAL
Procedure: Lung surgery

Interventions

Lung surgeryPROCEDURE
Pulmonary cancer

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients of 18 to 75 years of age.
  • Patients admitted for lung resection (either cancerous or non-cancerous) or lung transplant

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

CHU de Poitiers, Chirurgie Cardiaque et Thoracique

Poitiers, 86000, France

Location

Hopital Foch

Suresnes, Île-de-France Region, 92150, France

Location

MeSH Terms

Conditions

Lung NeoplasmsPulmonary Disease, Chronic ObstructiveEmphysema

Interventions

Pulmonary Surgical Procedures

Condition Hierarchy (Ancestors)

Respiratory Tract NeoplasmsThoracic NeoplasmsNeoplasms by SiteNeoplasmsLung DiseasesRespiratory Tract DiseasesLung Diseases, ObstructiveChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Thoracic Surgical ProceduresSurgical Procedures, Operative

Study Officials

  • Stanislas Grassin Delyle

    Hôpital Foch

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 19, 2013

First Posted

September 24, 2013

Study Start

August 1, 2011

Primary Completion

March 1, 2014

Study Completion

March 1, 2014

Last Updated

May 3, 2016

Record last verified: 2016-05

Locations