Hereditary Angioedema Kininogen Assay
NCT04091113 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 59
Last updated 2022-03-10
Summary
A multicenter epidemiological observational study aiming to explore the cleaved high-molecular weight kininogen (cHMWK) including identification and characterization of other metabolite/biomarkers in HAE type 1/2 patients
Conditions
Sponsors & Collaborators
-
CENTOGENE GmbH Rostock
lead INDUSTRY
Principal Investigators
-
Peter Bauer, MD · Centogene GmbH
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-09-01
- Primary Completion
- 2021-09-12
- Completion
- 2021-12-31
Countries
- Germany
Study Locations
More Related Trials
-
Monogenic Kidney Stone - Genetic Testing
NCT03305835 ·Status: RECRUITING
-
Prevalence of May-Thurner Syndrome in 1st-degree Relatives of Symptomatic Patients
NCT05409781 ·Status: WITHDRAWN
-
A Study on the Prevalence of Mutation of Cerebrotendinous Xanthomatosis (CTX)
NCT04218006 ·Status: UNKNOWN
-
Method of Genetic Analysis in Genodermatoses
NCT03873285 ·Status: UNKNOWN ·Phase: NA
-
Genomic First Testing in Chronic Kidney Disease
NCT06794567 ·Status: NOT_YET_RECRUITING
-
Genetic Basis of Hemangiomas
NCT00466375 ·Status: TERMINATED
-
Von Hippel-Lindau Disease Genetic Epidemiology Study
NCT00001803 ·Status: TERMINATED
-
Genetics of Rheumatoid Arthritis
NCT00001678 ·Status: COMPLETED
-
The Genetics of Kidneys in Diabetes (GoKinD) Study
NCT00024921 ·Status: COMPLETED
-
CABP2 Patient Registry and Natural History Study
NCT06680934 ·Status: RECRUITING
-
Genetics in the Progression of Nephropathies
NCT06416761 ·Status: RECRUITING
-
European Alpha-Mannosidosis Participant
NCT03651245 ·Status: TERMINATED
-
Observational Study of the Genetic Architecture of Neutrophil-Mediated Inflammatory Skin Diseases
NCT01952275 ·Status: UNKNOWN
-
Genetics of Charcot Marie Tooth (CMT) - Modifiers of CMT1A, New Causes of CMT2
NCT01193088 ·Status: RECRUITING
-
Genetics of Charcot-Marie-Tooth Dystrophy and Related Diseases
NCT04967716 ·Status: UNKNOWN
-
Identification of Genes Involved in Juvenile Idiopathic Arthritis by Wholel Exome Sequencing
NCT02067962 ·Status: COMPLETED ·Phase: NA
-
Gene Mutations and Orthopaedic Symptoms Correlation of Multiple Hereditary Exostoses: Multicentre Project
NCT00474331 ·Status: SUSPENDED
-
Studies of Hereditary Hemorrhagic Telangiectasia
NCT00004648 ·Status: COMPLETED
-
Genetic Study of Immunodeficiency: Search for New Genetic Causes for Primary Immunodeficiencies
NCT02735824 ·Status: RECRUITING
-
The Informed Genetics Annotated Patient Registry
NCT04419896 ·Status: ENROLLING_BY_INVITATION
-
Primary Premature Ejaculation Genetics
NCT02109302 ·Status: COMPLETED ·Phase: NA
-
Genetic and Functional Analysis of Craniometaphyseal Dysplasia (CMD)
NCT01630460 ·Status: RECRUITING
-
Pharmacogenetic Testing and Chronic Pain
NCT05259865 ·Status: SUSPENDED
-
Gene Polymorphisms Influencing Steroid Synthesis and Action
NCT00485186 ·Status: WITHDRAWN
-
Genetics of Ehlers-Danlos Syndrome
NCT03093493 ·Status: COMPLETED