Clinical Trials Logo

Epilepsies, Myoclonic clinical trials

View clinical trials related to Epilepsies, Myoclonic.

Filter by:

NCT ID: NCT02187809 Terminated - Dravet Syndrome Clinical Trials

Safety and Tolerability of Clobazam as Adjunctive Therapy in Paediatric Patients Aged ≥1 to ≤16 Years With Dravet Syndrome

Start date: March 2015
Phase: Phase 3
Study type: Interventional

To investigate the long-term safety and tolerability of clobazam when administered for 1 year as adjunctive therapy in paediatric patients aged ≥1 to ≤16 years with Dravet Syndrome.

NCT ID: NCT02174094 Withdrawn - Dravet Syndrome Clinical Trials

Clobazam as Adjunctive Therapy in Paediatric Patients Aged ≥1 to ≤16 Years With Dravet Syndrome

Start date: March 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the effect on the frequency of tonic-clonic and clonic seizures of clobazam as adjunctive therapy compared to placebo after 16 weeks of treatment in paediatric patients aged ≥1 to ≤16 years with Dravet Syndrome.

NCT ID: NCT02091375 Completed - Epilepsy Clinical Trials

Antiepileptic Efficacy Study of GWP42003-P in Children and Young Adults With Dravet Syndrome (GWPCARE1)

Start date: March 30, 2015
Phase: Phase 3
Study type: Interventional

To investigate the potential antiepileptic effects of cannabidiol (GWP42003-P) in children and young adults with Dravet syndrome.

NCT ID: NCT02091206 Completed - Epilepsy Clinical Trials

A Dose-ranging Pharmacokinetics and Safety Study of GWP42003-P in Children With Dravet Syndrome (GWPCARE1)

Start date: October 22, 2014
Phase: Phase 2
Study type: Interventional

To evaluate the safety and pharmacokinetics (PK) of multiple doses of GWP42003-P compared with placebo in children with Dravet syndrome.

NCT ID: NCT01983722 Approved for marketing - Dravet Syndrome Clinical Trials

Treatment Plan to Provide Expanded Access to Stiripentol for Patients With Dravet Syndrome

Start date: n/a
Phase:
Study type: Expanded Access

Expanded access to Stiripentol for patients with Dravet Syndrome.

NCT ID: NCT01858285 Recruiting - Epilepsy Clinical Trials

Genetics of Epilepsy and Related Disorders

Start date: November 2010
Phase:
Study type: Observational

Investigators at Boston Children's Hospital are conducting research in order to better understand the genetic factors which may contribute to epilepsy and related disorders. These findings may help explain the broad spectrum of clinical characteristics and outcomes seen in people with epilepsy.

NCT ID: NCT01835314 No longer available - Dravet Syndrome Clinical Trials

Compassionate Use of Stiripentol in Dravet Syndrome

Start date: n/a
Phase:
Study type: Expanded Access

Compassionate use of Stiripentol in Dravet Syndrome. This is a treatment protocol, not a research study, therefore children will only be monitored on a clinical basis for seizure improvement predominantly by parent and caregiver report.

NCT ID: NCT01607073 Completed - Dravet Syndrome Clinical Trials

Verapamil as Therapy for Children and Young Adults With Dravet Syndrome

Start date: April 2012
Phase: Phase 2
Study type: Interventional

This study will assess how well the drug verapamil can improve control of seizures and dysautonomia symptoms in children and young adults diagnosed with Dravet syndrome. The safety of verapamil when given with all concomitant medications will also be assessed.

NCT ID: NCT01533506 No longer available - Dravet Syndrome Clinical Trials

Stiripentol in Dravet Syndrome

Start date: February 2012
Phase: Phase 4
Study type: Expanded Access

The patient has failed all other available agents and has intractable epilepsy due to Dravet Syndrome. Stiripentol is highly efficacious in Dravet Syndrome. The overall goals of therapy with Stiripentol are primarily to significantly reduce the frequency and severity of seizures.

NCT ID: NCT01450423 Recruiting - Epilepsy Clinical Trials

Physical Exercise in Subjects With Juvenile Myoclonic Epilepsy

EFA
Start date: September 2011
Phase: Phase 2
Study type: Interventional

Epilepsy is a chronic neurologic disorder characterized by seizures. Beside seizures people suffering from epilepsy experience several challenges related to education, work and everyday life such as learning-, problem-solving-, memory-, concentration-, attention difficulties and fatigue. It is generally approved that physical activity (PA) has a positive effect on physical as well as mental factors. However, people with epilepsy are found to be less active and PA is rarely offered or recommended as supplement to anti-epileptic medical treatment. Few studies have investigated the effect of PA in subjects with epilepsy and additional studies of high methodical quality are needed to enable evidence-based information and counselling. This study is carried through as a randomized controlled trial which investigates the effect of participation in a 10-week cardio exercise program in people with Juvenile Myoclonic Epilepsy aged 15-50. The study hypothesis is that participation in a 10-week cardio exercise program will induce a positive change in cognitive function (concentration and attention) and possibly in brain-derived neurotrophic factor (BDNF). In addition it is expected that the intensity and duration of the 10-week cardio exercise program is sufficient to cause changes in physiological parameters related to a reduced risk of lifestyle diseases.