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Clinical Trial Summary

The purpose is to evaluate feasibility of medical supervision of professionally active asymptomatic wood workers with questionnaires and nasofibroscopy.

Secondary purposes are:

- Feasibility evaluation of identification of former and actual professional expositions to wood dust and to various naso-sinusal carcinogenics in case of co-expositions (formaldehyde, chrome, nickel, leather)

- Description of abnormal symptoms identified by occupational doctor and needing an otorhinolaryngology test

- Description of results and examinations induced by nasofibroscopy in symptomatic or asymptomatic individuals: counting of naso-sinusal adenocarcinoma cases

- Evaluation of participation of workers retiring in 2 years after inclusion to medical supervision program

- Evaluation of information flow among different players

- Assessment of costs induced by this targeted screening: direct medical costs (screened pathologies, induced additional examinations…) and indirect costs for company (duration of worker absence for transfer, medical and additional examinations).


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT02884232
Study type Observational
Source Central Hospital, Nancy, France
Contact
Status Completed
Phase N/A
Start date June 2012
Completion date June 2016