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Results for “Early Infantile Epileptic Encephalopathy”

14 trials

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Showing 14 of 14 results

Not applicableWithdrawnNCT05462054
What this trial is testing

Natural History Study in Pediatric Patients with STXBP1 Encephalopathy with Epilepsy

Who this might be right for
STXBP1 Encephalopathy with Epilepsy
Capsida Biotherapeutics, Inc.
Not applicableStudy completedNCT04924153
What this trial is testing

A Natural History Study of Participants With Potassium Sodium-Activated Channel Subfamily T Member 1 (KCNT1)-Related Epilepsy

Who this might be right for
KCNT1-Related Epilepsy
Biogen 35
Not applicableNot Yet RecruitingNCT07585643
What this trial is testing

IBIS - Investigating Reliability of BIS and SEDLINE Monitoring in Children With Developmental and Epileptic Encephalopathies (DEE).

Who this might be right for
Epileptic EncephalopathyEarly Infantile Epileptic EncephalopathyInfantile Spasm+1 more
Telethon Kids Institute 40
Not applicableLooking for participantsNCT06625112
What this trial is testing

A Multicentric European Study to Promote Clinical Trial Readiness for STXBP1-related Disorders

Who this might be right for
STXBP1 Encephalopathy With Epilepsy
European STXBP1 Consortium 120
Not applicableStudy completedNCT05161494
What this trial is testing

Gait in Rare Diseases

Who this might be right for
Tuberous SclerosisSTXBP1 Encephalopathy With Epilepsy
Universiteit Antwerpen 41
Large-scale testing (Phase 3)Active Not RecruitingNCT07010471
What this trial is testing

A Clinical Trial for Participants With DEE to Assess Efficacy, Safety, Tolerability, and PK of Relutrigine

Who this might be right for
Developmental and Epileptic Encephalopathy 1
Praxis Precision Medicines 160
Not applicableNot Yet RecruitingNCT06356233
What this trial is testing

Phenotyping and Identification of Biological Markers in STXBP1 Encephalopathy

Who this might be right for
STXBP1 Encephalopathy With Epilepsy
Fundación Iniciativa para las Neurociencias (FINCE) 10
Very early researchActive Not RecruitingNCT04937062
What this trial is testing

Phenylbutyrate for Monogenetic Developmental and Epileptic Encephalopathy

Who this might be right for
STXBP1 Encephalopathy With Epilepsy, SLC6A1 Neurodevelopmental DisorderDevelopmental and Epileptic Encephalopathy
Weill Medical College of Cornell University 50
Post-approval studies (Phase 4)UnknownNCT05232630
What this trial is testing

Fenfluramine for the Treatment of Different Types of Developmental and Epileptic Encephalopathies: a Pilot Trial Exploring Epileptic and Non-epileptic Outcomes

Who this might be right for
Refractory EpilepsySYNGAP1 EncephalopathySTXBP1 Encephalopathy With Epilepsy+3 more
Hospital Ruber Internacional 20
Not applicableEnrolling By InvitationNCT06938542
What this trial is testing

Palliative Care Needs of Children With Rare Diseases and Their Families

Who this might be right for
Trisomy 13 SyndromeArthrogryposis Congenita Multiplex With Intestinal AtresiaAsparagine Synthetase Deficiency+16 more
Children's National Research Institute 480
Not applicableStudy completedNCT02960347
What this trial is testing

Examining the Efficacy of tDCS in the Attenuation of Epileptic Paroxysmal Discharges and Clinical Seizures

Who this might be right for
Ohtahara Syndrome
Herzog Hospital 1
Not applicableLooking for participantsNCT01793168
What this trial is testing

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

Who this might be right for
Rare DisordersUndiagnosed DisordersDisorders of Unknown Prevalence+340 more
Sanford Health 20,000
Not applicableLooking for participantsNCT06555965
What this trial is testing

STXBP1 and SYNGAP1 Related Disorders Natural History Study

Who this might be right for
Genetic DiseaseSTXBP1 Encephalopathy With EpilepsySYNGAP1-Related Intellectual Disability
Children's Hospital of Philadelphia 600
Not applicableLooking for participantsNCT01238250
What this trial is testing

Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight

Who this might be right for
16P11.2 Deletion Syndrome16p11.2 Duplications1Q21.1 Deletion+184 more
Simons Searchlight 100,000