observation
OtherObservation of genetic characteristics
NCT Number: NCT05119387
The purpose of this study is to explore the genetic causes relevant for ALS development in Norway.
Interested in participating?
Request Info16 year–100 year
All sexes
Observational
Haukeland University Hospital, Department of Neurology, Bergen, Norway
After being informed about the study and potential risks, all patients giving written informed consent will be asked to complete a small questionnaire regarding family history and have a blood sample withdrawn. Blood samples, questionnaires, clinical information and signed consent is send to Department of Medical Genetics, Telemark Hospital Trust were the genetic analysis is performed successively throughout the recruitment period. Patients can choose to have their genetic results returned in a diagnostic setting.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Observation of genetic characteristics
Time frame: 2020-2030
Number of patients with disease causing mutations in high penetrant ALS genes
Time frame: 2024-2030
Identify new ALS genes in the Norwegian ALS population
Time frame: 2022-2030
Identify genetic risk factors for ALS in Norway.
Contact information is provided by the study sponsor or research team.
Sykehuset Telemark
Other Gov
Genetisk Studie av Amyotrofisk Lateral Sklerose (ALS)
Acronym: GAIN
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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