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NCT02266615 Clinical Trial

Biobank Clinical Genetics Maastricht (KG01)

Genetic Disease Clinical Trial

— KG01  

Official title:
Biobank Clinical Genetics Maastricht

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02266615
Other study ID # METC-14-4-077
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 2014
Est. completion date January 2035

Study information
Verified date October 2023
Source Maastricht University Medical Center
Contact I. Krapels, MD, PhD
Phone +31433875880
Email ingrid.krapels@mumc.nl
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Collection of coded biomaterial and clinical data with patients consent for future research.

Description:

Collection of coded biomaterial and clinical data with patients consent for future research, with the purpose to indentify new gene mutation and prossibilities for treatment in the future.

Recruitment information / eligibility
Status Recruiting
Enrollment 3600
Est. completion date January 2035
Est. primary completion date March 2024
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - New patients visiting the out patient clinic of the department of Clinical Genetics of the Maastricht University Medical Hospital - Withdrawal of body material for genetic diagnostics. Exclusion Criteria: - Patient does not understand the Dutch language.

Study Design

Related Conditions & MeSH terms

Intervention

Genetic:
• Biobanking of biomaterial for future genetic research.

Locations
Country Name City State
Netherlands Maastricht University Medical Center Maastricht Limburg

Sponsors (1)
Lead Sponsor Collaborator
Maastricht University Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome
Type Measure Description Time frame Safety issue
Primary Comparing genes to discover unknown functions The biobanked bio material and medical data can be used for future research to learn more about the function of genes. Genes will be sequenced and compared, within an expected average of 6 months.
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