Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ACTIVE_NOT_RECRUITING
25 participants
OBSERVATIONAL
2022-10-06
2025-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Use of Omics Methods to Classify Variations of Uncertain Significance and Improve Diagnosis of Neurogenetic Diseases
NCT06955624
Identification of the Genetic Causes of Rare Diseases With Negative Exome Findings
NCT04315727
NCGENES: North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing
NCT01969370
Investigating the Feasibility and Implementation of Whole Genome Sequencing in Patients With Suspected Genetic Disorder
NCT03829176
Diagnostic Value of Exome/ Genome Sequencing, Conventional Methods in Rare Diseases and Familial Tumor Syndromes
NCT04731857
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
However, a validated, reproducible, and broadly applicable tool to classify Gaucher Disease at any stage of the disease is still missing.
The development of new technologies, such as genomic analysis by next generation sequencing (NGS) and other "omics technologies," has advanced the molecular understanding and diagnosis of Rare Diseases
The current study will analyze the transcriptional and metabolomic profiles in blood, plasma and isolated monocytes from Gaucher patients and healthy controls with the aim to compare these profiles and to define how much a patient profile differs from a healthy one.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Gaucher Type 1
* The participant was diagnosed with Gaucher type 1 disease
* Adults only
Genetic testing and Omics analysis
Blood sample for genetic analysis and for Omics analysis as metabolomics and transcriptomics
Gaucher Type 3
* The participant was diagnosed with Gaucher type 3 disease
* Adults only
Genetic testing and Omics analysis
Blood sample for genetic analysis and for Omics analysis as metabolomics and transcriptomics
Healthy Volunteer
* Healthy participants
* Adults only
Genetic testing and Omics analysis
Blood sample for genetic analysis and for Omics analysis as metabolomics and transcriptomics
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Genetic testing and Omics analysis
Blood sample for genetic analysis and for Omics analysis as metabolomics and transcriptomics
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Informed consent
* The participant is older than 18 years old
* The participant was diagnosed with Gaucher Type 1 disease
Gaucher Type 3 participants:
* Informed consent
* The participant is older than 18 years old
* The participant was diagnosed with Gaucher type 3 disease
Healthy participants:
* Informed consent
* The participant is older than 18 years old
* Healthy participants
Exclusion Criteria
* The participant had any other clinically significant disease
* The participant had a recent (within 14 days) acute infection and/or vaccination
Gaucher Type 3 participants:
* Diagnosis of a significant CNS disease or cardiovascular disease other than Gaucher type 3
* The participant had a recent (within 14 days) acute infection and/or vaccination
Healthy participants:
* The participant had a recent (within 14 days) acute infection and/or vaccination
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
CENTOGENE GmbH Rostock
INDUSTRY
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Peter Bauer, MD
Role: PRINCIPAL_INVESTIGATOR
CENTOGENE GmbH
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
UKE
Hamburg, , Germany
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
OG 01-2022
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.