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Immunologically-induced Lung DiseaseNCT01487850

Wind Instruments' Fungal Contamination

A study testing blood sample in people with Immunologically-induced Lung Disease and Hypersensitivity Pneumonitis, run by Centre Hospitalier Universitaire de Besancon at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

On the basis of 2 cases of immunologically-induced lung disease in 2 saxophonists, the investigators supposed that wind reed instruments could be contaminated with molds. The investigators led a study on 40 musicians playing a wind reed instrument to analyze instruments' fungal contamination and its immunological and… Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
blood sample
How many people
Not given
Where
1 siteFrance
Study dates
May 2007to Oct 2007
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • must be 18 year old or more
  • must play a wind reed instrument (saxophone, clarinet, bassoon or oboe) one hour per week or more

Who cannot join

  • refuse to sign consent

Trial locations and contacts

1 site in 1 country.

France1 site
  • Centre Hospitalier Universitaire Saint Jacques

    Besançon, Franche Comté, 25000

Other trials in France

About this study

Official title: Study of Wind Reed Instruments' Fungal Contamination and Its Immunological and Clinical Consequences for Musicians.

On the basis of 2 cases of immunologically-induced lung disease in 2 saxophonists, the investigators supposed that wind reed instruments could be contaminated with molds. The investigators led a study on 40 musicians playing a wind reed instrument to analyze instruments' fungal contamination and its immunological and clinical consequences for musicians.

Being tested
blood sample
Keywords
wind instruments, molds, hypersensitivity pneumonitis, fungal contamination of wind instruments, specific antibodies against molds in musicians' sera, musicians
Medical subject headings
Alveolitis, Extrinsic Allergic

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • blood sampleBiological

    blood sample in each musician to search for specific antibodies against molds isolated from instruments

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Dec 2011 (estimated)
  2. Study startMay 2007
  3. Primary completionJun 2007
  4. Study completionOct 2007

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Diagnosis
IDs, dates and publications
ClinicalTrials.gov ID
NCT01487850
Sponsor's protocol ID
P/2007/55
Status last verified
Dec 2011
First submitted
6 Dec 2011
Last updated
9 Dec 2011
Results posted
No
Data monitoring committee
No

Publications

  • Lodha S, Sharma OP. Hypersensitivity pneumonitis in a saxophone player. Chest. 1988 Jun;93(6):1322. doi: 10.1378/chest.93.6.1322. No abstract available.

    PubMed 3371127
  • Metzger F, Haccuria A, Reboux G, Nolard N, Dalphin JC, De Vuyst P. Hypersensitivity pneumonitis due to molds in a saxophone player. Chest. 2010 Sep;138(3):724-6. doi: 10.1378/chest.09-2991.

    PubMed 20822994

Questions about this trial

What is this clinical trial studying?

A study testing blood sample in people with Immunologically-induced Lung Disease and Hypersensitivity Pneumonitis, run by Centre Hospitalier Universitaire de Besancon at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 9 Dec 2011. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01487850, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Dec 2011.

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