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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT02361281
Other study ID # BC/1408-389
Secondary ID
Status Enrolling by invitation
Phase N/A
First received February 2, 2015
Last updated February 6, 2015
Start date December 2014
Est. completion date July 2015

Study information

Verified date February 2015
Source Maastricht University
Contact n/a
Is FDA regulated No
Health authority Netherlands: Medical Ethics Review Committee (METC)
Study type Observational

Clinical Trial Summary

Sarcoidosis is a chronic lung disease that is characterized by fatigue, shortness of breath, chest pain and reduced lung function. Suffering from these diseases has a very negative effect on the quality of life. When people are suspected of having sarcoidosis various markers in the blood are measured. Ultimate diagnosis, however, always requires invasive techniques such as bronchoscopy and lung biopsy. Consequently, there is an urgent need for a new diagnostic tool that is easy, quick and most of all non-invasive and thus friendly for the patient.

Such a new diagnostic tool might be found in examining the exhaled air of patients, which contains a complex mixture of so-called volatile organic compounds (VOCs) that are the result of damaging processes that occur in the lung. Determining the VOC profile in the breath can be used as a biomarker, or biological indicator, of those damaging processes. In other words, searching for unique VOC profiles in the breath of sarcoidosis patients might lead to the development of a diagnostic tool that only uses their exhaled breath.

The current study involves 25 sarcoidosis patients and 25 healthy volunteers. The aim of this study is find VOCs in exhaled air that can be used to diagnose sarcoidosis. In a previous study, sarcoidosis-specific VOCs were found, which we intend to validate using the current study.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 50
Est. completion date July 2015
Est. primary completion date March 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients with confirmed sarcoidosis

Exclusion Criteria:

- (ex-) smokers

- for healthy controls: controls with pulmonary disease excluded

Study Design

Observational Model: Case Control, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
Maastricht University Atrium Medical Center, Gelderse Vallei Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary diagnosis by exhaled breath upon regular visit to clinic, which is expected to occur on average within 4 months after the start of the study No
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