Early Detection and Characterization of Primary Ciliary Dyskinesia
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|ClinicalTrials.gov Identifier: NCT01070914|
Recruitment Status : Unknown
Verified May 2012 by Ziv Hospital.
Recruitment status was: Recruiting
First Posted : February 18, 2010
Last Update Posted : May 8, 2012
|Condition or disease|
|Primary Ciliary Dyskinesia|
Primary Ciliary Dyskinesia (PCD) is a severe genetic disorder caused by various mutations in genes affecting ciliary motility. While diagnosis of PCD in Israel is currently based for the most part on electron microscopy (EM) detection of ciliary ultrastructural defects, this technique may be unsatisfactory and does not overcome the inherent heterogeneity. Thus, late and under-diagnosis and suboptimal characterization of patients is common. Various newer and complementary diagnostic techniques, including measurements of nasal nitric oxide (NO), Video Microscopy (VM), Immunoflourescence (IF) and genetic analysis have recently been recognized as simpler and more accurate modalities for the diagnosis and characterization of patients with PCD. While considered a rare disease worldwide, PCD is more prevalent among highly consanguineous populations, such as those found in Israel. Given the rarity of cases particularly familial ones, the most useful implementation of new diagnostic techniques requires multicenter collaboration.
We hypothesize that using modern state of the art and novel test modalities on a national scale in Israel will improve diagnosis, improve phenotypic-genotypic correlations and create a national registry for PCD.
We propose to perform such a multicenter study whose aims are:
- To characterize the complex phenotype and genotype of PCD in Israel, using state-of-the-art and novel diagnostic techniques.
- To create a national registry of patients and families with PCD in Israel
- To develop robust national standards of diagnosis and evaluation, which will lead to better and earlier diagnosis, treatment and counseling.
|Study Type :||Observational|
|Estimated Enrollment :||130 participants|
|Official Title:||The Israeli National Consortium for Early Detection and Characterization of Primary Ciliary Dyskinesia|
|Study Start Date :||June 2011|
|Estimated Primary Completion Date :||December 2012|
|Estimated Study Completion Date :||June 2013|
- Phenotypic and genetic characterization [ Time Frame: 2 years ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01070914
|Contact: Israel Amirav, MDfirstname.lastname@example.org|
|Ziv Medical center||Recruiting|
|Safed, Israel, 13100|
|Principal Investigator: Israel Amirav, MD|
|Principal Investigator:||Israel Amirav, MD||Ziv Medical Center|