- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01809145
Testing Hypersensitivity to Metals in Sarcoidosis Patients by Applying the MELISA Test.
March 10, 2013 updated by: Tel-Aviv Sourasky Medical Center
Testing Hypersensitivity to Metals in Sarcoidosis Patients With Occupational Exposure, Using the MELISA Test.
The purpose of this study is to apply the MELISA test, that diagnose hypersensitivity to metals, in Sarcoidosis patients with occupational exposure.
Study Overview
Detailed Description
Peripheral blood from sarcoidosis patients with occupational anamnesis that involves exposure to metals will be sent to MELISA Medica in Stockholm Sweden.
The MELISA test will examine hypersensitivity to metals that can be related to the granulomatous response of sarcoidosis.
Study Type
Interventional
Enrollment (Anticipated)
10
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Tel Aviv, Israel, 64239
- Recruiting
- Tel-Aviv Sourasky Medical Center
-
Contact:
- Elizabeth Fireman, PhD
- Phone Number: 972-36973988
- Email: fireman@tlvmc.gov.il
-
Contact:
- Yifat Alcalay, PhD
- Phone Number: 973-36973749
- Email: yifatal@tlvmc.gov.il
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
Biopsy confirmed sarcoidosis Granulomatous disease Occupational anamnesis with exposure to metals
Exclusion Criteria:
Patients with interstitial disease No occupational anamnesis
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: metal hypersensitivity
peripheral blood test for metal hypersensitivity (MELISA test)
|
MELISA test for hypersensitivity to metals in sarcoidosis
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
MELISA test
Time Frame: 30 days
|
Using the MELISA test in peripheral blood, in order to find hypersensitivity to metals that can be related to the granulomatous response of sarcoidosis.
|
30 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Elizabeth Fireman, PhD, Tel-Aviv Sourasky Medical Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2013
Primary Completion (Anticipated)
December 1, 2013
Study Completion (Anticipated)
December 1, 2013
Study Registration Dates
First Submitted
March 7, 2013
First Submitted That Met QC Criteria
March 10, 2013
First Posted (Estimate)
March 12, 2013
Study Record Updates
Last Update Posted (Estimate)
March 12, 2013
Last Update Submitted That Met QC Criteria
March 10, 2013
Last Verified
March 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- TASMC-13-LF-0683-CTIL
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Sarcoidosis
-
Mayo ClinicNot yet recruitingCardiac Sarcoidosis | Sarcoidosis, Cardiac | Sarcoidosis With Myocarditis | Sarcoidosis of the HeartUnited States
-
Celularity IncorporatedTerminatedStage 2 Pulmonary Sarcoidosis | Stage 3 Pulmonary SarcoidosisUnited States
-
Vanderbilt UniversityNational Heart, Lung, and Blood Institute (NHLBI)CompletedSarcoidosis; Antimycobacterial TherapyUnited States
-
Duke UniversityFoundation for Sarcoidosis ResearchRecruiting
-
Sanjay Gandhi Postgraduate Institute of Medical...RecruitingSarcoidosis Lung | Pulmonary SarcoidosisIndia
-
Alexandria UniversityCompletedEndobronchial Mucosal Pathology in Pulmonary SarcoidosisEgypt
-
Heart Center Leipzig - University HospitalRecruiting
-
British Columbia Cancer AgencyApproved for marketing
-
University of Maryland, BaltimoreMallinckrodtCompleted
-
University of PennsylvaniaAdvanced Accelerator ApplicationsCompleted
Clinical Trials on MELISA test
-
Centre Hospitalier Universitaire de Saint EtienneRecruitingInfantile Spinal Muscular Atrophy | Spinal Amyotrophy | Juvenile Spinal Muscular AtrophyFrance
-
Groupe Hospitalier Mutualiste de GrenobleFondation de l'AvenirCompleted
-
Recep Tayyip Erdogan University Training and Research...Completed
-
Yonsei UniversityCompletedPostprandial Hyperglycemia
-
University of FloridaCompletedParkinson Disease (PD)United States
-
Clinical Nutrition Research Centre, SingaporeCompleted
-
French National Agency for Research on AIDS and...Completed
-
Guven Health GroupCompletedAthletic Performance | Physical Fitness | Handball Players | Cross-sectional StudiesTurkey
-
University of MichiganCompletedAntidepressants Causing Adverse Effects in Therapeutic UseUnited States