A Study to Gather Information About Overall Occurrence and New Cases of Dravet and Lennox-Gastaut Syndromes in Children, Teenagers and Adults in Spain

Dravet Syndrome (DS) Clinical Trial

— DRALEGA  

Official title:

Epidemiology of Dravet and Lennox-Gastaut Syndromes in Spain

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05982717
• Other study ID #: TAK-935-5003
• Status: Recruiting
• Start date: October 26, 2023
• Est. completion date: May 31, 2024

Study information

• Verified date: March 2024
• Source: Takeda
• Contact: Takeda Contact
• Phone: +1-877-825-3327
• Email: medinfoUS[@]takeda.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The main aims of this study are to gather information about how many children, teenagers and adults in Spain have been diagnosed with Dravet syndrome and Lennox-Gastaut syndrome as well as to learn about the number of new Dravet syndrome and Lennox-Gastaut syndrome cases in persons in Spain.

Participants' data will be taken from their medical records (charts), which were already collected as a part of their routine care in public hospitals in Spain between 01 January 2021 and 31 December 2022.

Description:

This is a non-interventional, retrospective study of participants from Spain with DS and LGS at public hospitals. The participants will be identified from their medical charts or hospital records and those who meet the eligibility criteria will be included.

This multi-center trial will be conducted in Spain. Data will be retrospectively collected for the observation period between 01 January 2021 to 31 December 2022. The total duration of the study is approximately 24 months.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 250
• Est. completion date: May 31, 2024
• Est. primary completion date: May 31, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

A. Diagnosis criteria for DS:

• All the following criteria must be met: i. Seizures onset within 1-20 months (usually within the first year of life). ii. Normal initial development prior to presentation (no cognitive or behavioural disability before the onset of seizures) followed by behaviour and cognitive impairment.

iii. Recurrent focal clonic (hemiclonic) febrile and afebrile seizures (which often alternate sides from seizure to seizure), focal to bilateral tonicclonic, and/or generalized clonic seizures.

• And at least one of the following criteria must be met: i. Emergence of other seizure type, including atypical absence seizures, myoclonic seizures, atonic seizures, or non-tonic-clonic status epilepticus between 1-4 years.

ii. Seizures triggered by fever due to illness or vaccinations, hot baths, sudden temperature changes, high level of activity, or by strong lighting or exposure to certain visual patterns.

iii. Mutations or copy number variants in the SCN1A gene.

B. Diagnosis criteria for LGS:

Given the uncertainties associated with the diagnosis of this condition, two different criteria will be used, a stricter criterion, intended to identify "pure" Lennox-Gastaut syndrome participants, and a wider criterion, intended to also include the so-called Lennox-Gastaut-like participants.

Lennox-Gastaut syndrome - stricter criteria:

• All the following criteria must be met: i. Seizures onset before 18 years of age, typically from 1 to 8 years. ii. Progressive development/cognition impairment after seizures onset. iii. Tonic seizures. iv. At least one additional seizure: generalised tonic-clonic seiures, atypical absence seizures, atonic seizures, myoclonic seizures, focal impaired awareness, epileptic spams, or non-convulsive status epilepticus v. Slow (<2.5 hertz [Hz]) spike-and-wave EEG pattern. vi. Paroxysmal fast activity (10 Hz or greater) in sleep.

Lennox-Gastaut syndrome - wider criteria:

• At least one the following criteria must be met:

i. Tonic seizures. ii. Multiple types of seizures, including generalised tonic-clonic seizures, atypical absence seizures, atonic seizures, myoclonic seizures, myoclonic-atonic seizures, focal seizures, epileptic spams, or nonconvulsive status epilepticus.

• And at least one the following criteria must be met:

i. Slow (<2.5 Hz) spike-and-wave EEG pattern. ii. Paroxysmal fast activity (10 Hz or greater) in sleep.

• And at least two of the following criteria must be met:

i. Seizures onset before 18 years of age, typically from 1 to 8 years. ii. Progressive development/cognition impairment after seizures onset. iii. Development/cognition impairment starts prior to seizures onset. iv. History of Infantile epileptic spasms syndrome (IESS), West or Ohtahara syndromes.

Exclusion Criteria

1. Participants with epileptic condition other than DS or LGS.

2. Participants with DS or LGS not residents in the reference area of the hospital.

Related Conditions & MeSH terms

• Epilepsies, Myoclonic
• Lennox Gastaut Syndrome
• Lennox-Gastaut Syndrome (LGS)
• Syndrome

Intervention

Other:
• No intervention
As this is an observational study, no intervention will be administered.

Locations

Country	Name	City	State
Spain	H. Universitario Infantil Niño Jesús	Madrid
Spain	H. Universitario La Paz	Madrid
Spain	Hospital Universitari i Politècnic La Fe	Valencia
Spain	Complejo Hospitalario Universitario de Vigo	Vigo	Pontevedra

Sponsors (1)

Lead Sponsor	Collaborator
Takeda

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	One-Year Period Prevalence of DS	Number of participants with DS over a period of one year will be assessed.	Up to 12 months
Primary	Incidence of DS	Number of new participants diagnosed annually with DS yearly.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Primary	One-Year Period Prevalence of LGS Based on Stricter Diagnosis Criterion	Number of participants with LGS over a period of one year based on stricter diagnosis criterion will be assessed.	Up to 12 months
Primary	Incidence of LGS Based on Stricter Diagnosis Criterion	Number of new participants diagnosed annually with LGS based on stricter diagnosis criterion.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	One-Year Period Prevalence of LGS Based on Wider Diagnosis Criterion	Number of participants with LGS over a period of one year based on wider diagnosis criterion will be assessed.	Up to 12 months
Secondary	Incidence of LGS Based on Wider Diagnosis Criterion	Number of new participants diagnosed annually with LGS based on wider diagnosis criterion.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	One-Year Period Prevalence of Paediatric DS	Number of participants with paediatric DS over a period of one year will be assessed.	Up to 12 months
Secondary	One-Year Period Prevalence of Paediatric LGS Based on Stricter and Wider Diagnoses Criteria	Number of participants with paediatric LGS over a period of one year based on stricter and wider diagnoses criteria will be assessed.	Up to 12 months
Secondary	One-Year Period Prevalence of Adult DS	Number of participants with adult DS over a period of one year will be assessed.	Up to 12 months
Secondary	One-Year Period Prevalence of Adult LGS Based on Stricter and Wider Diagnoses Criteria	Number of participants with adult LGS over period of one year based on stricter and wider diagnoses criteria will be assessed.	Up to 12 months
Secondary	Incidence of Paediatric DS	Number of new paediatric participants diagnosed annually with DS.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	Incidence of Paediatric LGS Based on Stricter and Wider Diagnoses Criteria	Number of new paediatric participants diagnosed annually with LGS based on stricter and wider diagnoses criteria.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	Incidence of Adult DS	Number of new adult participants diagnosed annually with DS.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	Incidence of Adult LGS Based on Stricter and Wider Diagnoses Criteria	Number of new adult participants diagnosed annually with LGS based on stricter and wider diagnoses criteria.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	DS Categorized Based on Gender Distribution		Up to 12 months
Secondary	LGS Categorized Based on Gender Distribution According to Stricter and Wider Diagnoses Criteria		Up to 12 months
Secondary	DS Categorized Based on Age Distribution		Up to 12 months
Secondary	LGS Categorized Based on Age Distribution According to Stricter and Wider Diagnoses Criteria		Up to 12 months
Secondary	DS Categorized Based on Gender Distribution at Diagnosis	Annually diagnosed DS participants will be categorized based on gender distribution at diagnosis.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	LGS Categorized Based on Gender Distribution at Diagnosis According to Stricter and Wider Diagnoses Criteria	Annually diagnosed LGS participants will be categorized based on gender distribution at diagnosis.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	DS Categorized Based on Age Distribution at Diagnosis	Annually diagnosed DS participants will be categorized based on age distribution at diagnosis.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	LGS Categorized Based on Age Distribution at Diagnosis According to Stricter and Wider Diagnoses Criteria	Annually diagnosed LGS participants will be categorized based on age distribution at diagnosis.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	DS Categorized Based on Gender Distribution at Symptoms Onset	Annually diagnosed DS participants will be categorized based on gender distribution at symptoms onset.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	LGS Categorized Based on Gender Distribution at Symptoms Onset According to Stricter and Wider Diagnoses Criteria	Annually diagnosed LGS participants will be categorized based on gender distribution at symptoms onset.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	DS Categorized Based on Age Distribution at Symptoms Onset	Annually diagnosed DS participants will be categorized based on age distribution at symptoms onset.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	LGS Categorized Based on Age Distribution at Symptoms Onset According to Stricter and Wider Diagnoses Criteria	Annually diagnosed LGS participants will be categorized based on age distribution at symptoms onset.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	Diagnosis Delay for Participants With DS	Diagnosis delay is defined as time from symptoms onset to diagnosis.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	Diagnosis Delay for Participants With LGS Based on Stricter and Wider Diagnoses Criteria	Diagnosis delay is defined as time from tonic seizures onset to electroencephalography (EEG) confirmation.	At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	Participants With DS: Ratio of Participants Genetically (Sodium Channel Protein Type 1 Subunit Alpha [SCN1A] Mutation) and Clinically Diagnosed Versus Participants Clinically Diagnosed Only		At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	Participants With LGS: Number of Participants Distributed According to Aetiologies Based on Stricter and Wider Diagnoses Criteria		At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	Participants With DS: Number of Participants With Different Types of Comorbidities at Diagnosis		At two different 12 month periods (in consecutive years at Months 12 and 24)
Secondary	Participants With LGS: Number of Participants With Different Types of Comorbidities at Diagnosis Based on Stricter and Wider Diagnoses Criteria		At two different 12 month periods (in consecutive years at Months 12 and 24)

External Links

•   To obtain more information on the study, click this link.