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The study aims to characterize prospectively longitudinal progression of neurological domains in GM1 and GM2 Gangliosidosis patients with high-quality standards (GCP compliant).
The study is a prospective longitudinal, multicentric decentralized trial which will be performed in children diagnosed with late infantile or juvenile onset of neurological disease of either GM1 or GM2 Gangliosidoses (Tay-Sachs or Sandhoff disease). The study anticipates to include a total of approximately 35 patients. A large set of neurological functions will be evaluated by rating scales used by physicians and questionnaires answered by parents. Digital tools will be used to support the study procedures with virtual visits.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Cohort | Late infantile or juvenile onset for GM1 or GM2 Gangliosidosis. The study anticipates to include a total of approximately 35 patients. |
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| Measure | Description | Time Frame |
|---|---|---|
| Change in the Gait 9-point item score of the Scale for Assessment and Rating of Ataxia (SARA) | Score between 0 (better) and 8 (worse) points | 0-4 years |
| Change in the Speech 7-point item score of SARA | Score between 0 (better) and 6 (worse) points | 0-4 years |
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| Measure | Description | Time Frame |
|---|---|---|
| Change in scores of SARA items Stance (7-point), Sitting (5-point), Finger chase (5-point), Nose-finger test (5-point), Fast alternating hand movement (5-point), Heel-shin slide (5-point) and overall score. | Stance score between 0 (better) and 6 (worse) points Sitting score between 0 (better) and 4 (worse) points Finger chase test score between 0 (better) and 4 (worse) points Nose-finger test score between 0 (better) and 4 (worse) points Fast alternating hand movements test score between 0 (better) and 4 (worse) points Heel-shin slide score between 0 (better) and 4 (worse) points |
Inclusion Criteria:
Exclusion Criteria:
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Individuals with diagnosis of GM1 Gangliosidosis Tay-Sachs disease, or Sandhoff disease, or late infantile or juvenile onset of neurological disease
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| UCSF Benioff Children's Hospital | Oakland | California | 94609 | United States | ||
| Mayo Clinic Rochester |
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| ID | Term |
|---|---|
| D016537 | Gangliosidosis, GM1 |
| D012497 | Sandhoff Disease |
| D013661 | Tay-Sachs Disease |
| D020143 | Gangliosidoses, GM2 |
| D016464 | Lysosomal Storage Diseases |
| D009422 | Nervous System Diseases |
| D030342 | Genetic Diseases, Inborn |
| ID | Term |
|---|---|
| D005733 | Gangliosidoses |
| D013106 | Sphingolipidoses |
| D020140 | Lysosomal Storage Diseases, Nervous System |
| D020739 | Brain Diseases, Metabolic, Inborn |
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| 0-4 years |
| Change in the total score of the Motor Function Measure-32 (MFM-32), and each of the 3 domains | The scoring of each item uses a 4-point Likert scale - score between 0 (worse) and 3 (better) | 0-4 years |
| Change of Timed Up & Go | Time a patient takes to rise from a chair, walk 3 meters, turn around 180°, walk back to the chair, and sit down while turning 180° | 0-4 years |
| Change in swallowing score | Assessment of patient swallowing ability - score between 0 (better) and 5 (worse) | 0-4 years |
| Change in the overall composite score of the Vineland Adaptive Behavioral Scale (VABS) | Rated on 0 (never performed),1, 2 (habitually performed) scale | 0-4 years |
| Change in BSFC-s score for each of the 10 items and overall score | Rated on a 4-point scale with the values "strongly disagree", "disagree", "agree", and "strongly agree" | 0-4 years |
| Collection of seizures events, choking episodes, respiratory tract infections | Gathering data about presence/absence and frequency of seizures, choking episodes, respiratory tract infections | 0-4 years |
| Rochester |
| Minnesota |
| 55905 |
| United States |
| Hospital Pequeno Principe | Curitiba | Brazil |
| Hospital de Clinicas de Porto Alegre | Porto Alegre | Brazil |
| Hopital d'Enfants CHU Timone | Marseille | France |
| Armand-Trousseau Children's Hospital - CHU Paris Est | Paris | France |
| Hôpital des Enfants - CHU Toulouse Purpan | Toulouse | France |
| Universtitäsklinikum Giessen und Marburg | Giessen | Germany |
| LMU - Klinikum der Universitaet Muenchen - Neurologische Klinik und Poliklinik | Munich | Germany |
| Universita' di Catania | Catania | Italy |
| Fondazione IRCCS Istituto Neurologico Carlo Besta | Milan | Italy |
| University Hospital Friuli Centrale | Udine | Italy |
| Great Ormond Street Hospital NHSFT | London | United Kingdom |
| D001928 | Brain Diseases, Metabolic |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D008661 | Metabolism, Inborn Errors |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D008064 | Lipidoses |
| D008052 | Lipid Metabolism, Inborn Errors |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D052439 | Lipid Metabolism Disorders |