Telomeres Parameters in Celiac Disease
NCT02126033 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40
Last updated 2014-04-29
Summary
Celiac disease is an autoimmune process that causes destructive changes in the epithel of the small bowel and it is also a pre-malignant state (e.g lymphoma). The aim of the study is to examine telomere length and other parameters of genetic instability from peripheral blood lymphocytes of patients with celiac disease compared with healthy controls.
Conditions
Interventions
- PROCEDURE
-
take blood samples
Sponsors & Collaborators
-
Meir Medical Center
lead OTHER
Study Design
- Purpose
- BASIC_SCIENCE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Primary Completion
- 2015-12-31
More Related Trials
-
The Natural History of Reproductive and Overall Health in Girls and Women With a Pre-Mutation in the FMR1 Gene; Creation of a Patient Registry
NCT01187524 ·Status: TERMINATED
-
Identification of Genes Involved in Juvenile Idiopathic Arthritis by Wholel Exome Sequencing
NCT02067962 ·Status: COMPLETED ·Phase: NA
-
Next Generation Sequencing Analysis of Patients with Spontaneous Dissection of Cervical Arteries
NCT06862063 ·Status: RECRUITING ·Phase: NA
-
Study of Congenital Orofacial Clefts by Implementing Optical Genome Mapping
NCT06880094 ·Status: RECRUITING ·Phase: NA
-
Evaluation of Patients With Unresolved Chromosome Abnormalities
NCT00001639 ·Status: COMPLETED
-
Next Generation Sequencing Diagnostics - On the Road to Rapid Diagnostics for Rare Diseases
NCT02588638 ·Status: UNKNOWN
-
X-linked Moesin Associated Immunodeficiency
NCT06278337 ·Status: RECRUITING
-
NIAID Clinical Center Genomics Opportunity Protocol
NCT02417766 ·Status: COMPLETED
-
Genetic Analysis of Neural Tube and Orofacial Cleft Defects in the Irish Population
NCT00341068 ·Status: TERMINATED
-
Genetic Study of Immunodeficiency: Search for New Genetic Causes for Primary Immunodeficiencies
NCT02735824 ·Status: RECRUITING
-
FaceBase Biorepository
NCT01252264 ·Status: COMPLETED
-
Genetic and Immunologic Characterization of IEI
NCT05803356 ·Status: COMPLETED
-
Longitudinal Studies of Patient With FPDMM
NCT03854318 ·Status: RECRUITING
-
Neurologic and Immunologic Characteristics of CTLA-4 and LRBA Hereditary Deficiency
NCT05040256 ·Status: COMPLETED
-
Immune Biomarkers Related to Bone Pathology in Patients With Type 1 Gaucher Disease
NCT04055831 ·Status: UNKNOWN
-
Limbal Stem Cell Deficiency of Genetic Origin: Genotype-phenotype Correlation
NCT02886611 ·Status: RECRUITING
-
LeukoSEQ: Whole Genome Sequencing as a First-Line Diagnostic Tool for Leukodystrophies
NCT02699190 ·Status: COMPLETED
-
Observational Study of the Genetic Architecture of Neutrophil-Mediated Inflammatory Skin Diseases
NCT01952275 ·Status: UNKNOWN
-
Biomarkers in Rett Syndrome
NCT06346444 ·Status: RECRUITING
-
Prevalence of May-Thurner Syndrome in 1st-degree Relatives of Symptomatic Patients
NCT05409781 ·Status: WITHDRAWN
-
A Clinical Study to Map the HLA Genomic Region in the Greek Population
NCT06227468 ·Status: RECRUITING
-
Disease Characteristics and Treatment Response in Plasma Cell Disorders Patients Based on Genetic Abnormalities From Fluorescence In Situ Hybridization and Next Generation Sequencing
NCT06330896 ·Status: NOT_YET_RECRUITING
-
Genetic Analysis of Hereditary Non-Syndromic Oral Clefts
NCT00340626 ·Status: COMPLETED
-
Genetic Analysis of Uncommon Disease Presentations in Non-US Populations
NCT06595940 ·Status: RECRUITING
-
Phenotypic and Genotypic Identification and Characterization of MYH9-related Constitutional Thrombocytopenia
NCT00925236 ·Status: COMPLETED