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Spasms, Infantile clinical trials

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NCT ID: NCT06315829 Not yet recruiting - Infantile Spasms Clinical Trials

Artificial Intelligence-based Video Analysis to Detect Infantile Spasms

Start date: August 2024
Phase:
Study type: Observational

Infantile spasms are a type of seizure linked to developmental issues. Unfortunately, they are often misdiagnosed, causing delays in treatment. The purpose of this study is to develop a computer program that can reliably differentiate infantile spasms from similar, yet benign movements in videos. This computer program will learn from videos taken by parents of study participants. Quickly recognizing and treating infantile spasms is crucial for ensuring the best developmental outcomes.

NCT ID: NCT05462054 Not yet recruiting - Clinical trials for STXBP1 Encephalopathy With Epilepsy

Natural History Study in Pediatric Patients With STXBP1 Encephalopathy With Epilepsy

Start date: July 2023
Phase:
Study type: Observational

This is a prospective, non-interventional, longitudinal study designed to characterize the natural history of STXBP1 related encephalopathy with epilepsy, in participants ≤ <5 years of age.

NCT ID: NCT05126914 Not yet recruiting - Epilepsy Clinical Trials

Multicentre Real-life Follow-up Study of Rare Epileptic Syndromes in Children and Adolescents

EPIRARE
Start date: December 2021
Phase:
Study type: Observational

Rare epilepsies as a whole account for 20-30% of epilepsies, but knowledge about prognostic factors is currently limited. This means that it is difficult to provide adequate information to families at diagnosis and during follow-up. Prognostic factors are also important for management as they can have an impact on the patient's outcome (time to intervention, choice of one molecule over another, etc.). Finally, few treatments are currently available for these epilepsies. One of the limitations to the development of treatments is the lack of real life data as it is difficult to create reliable primary endpoints such as the rate of patients becoming seizure free naturally compared to a therapeutic intervention. The aim of this real-life study is to evaluate the response to treatment as well as to see the evolution of cognitive and psychiatric comorbidities. As explained above, there are very few randomised trials except for 3 rare epilepsies (infantile spasm syndrome, Dravet syndrome, Lennox-Gastaut syndrome). This has led to the virtual absence of management recommendations, including for the three syndromes mentioned above, where attempts at treatment algorithms have been proposed, although these have not been able to be considered as evidence-based recommendations. As a result, there is some diversity in the management of rare epilepsies from one centre to another. However, this diversity in management can be an asset in a real-life study. This will make it possible to compare different management methods, both in terms of seizure control and medium-term outcome.