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NCT Number: NCT06792396

Study of Patients with Electrical Status Epilepticus in Sleep

Our aims are:

1. To understand the diagnostic practices, treatment and long term management and outcomes for patients diagnosed with ESES locally. 2. To establish a regional and national guideline for the diagnosis and management of patients with ESES.

The secondary questions that can be addressed with this case series review include the variability of clinical care given to patients with this condition, and for example, the duration of time it takes to obtain diagnostic tests and assessments by psychologists.

Recruiting

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Key information

Age range

1 year–16 year

Sex eligibility

All sexes

Study type

Observational

Primary location

East Suffolk and North Essex NHS Foundation Trust

Colchester, United Kingdom

Location status: Recruiting

Location contact

Thiloka Ratnaike

CONTACT

R&[email protected]

01473 704343

About this study

The Paediatric consultants specialising in epilepsy and neurodisability at ESNEFT that are on the delegation log will identify patients who have been diagnosed with ESES since 2010.

This list of patients will be pseudo-anonymised (by tagging patients with a random identification number). Patient identifiable data including local hospital identification number and date of birth will be collected on the local case record form (CRF) to enable retrospective data collection. The hospital number will remain within the Trust, meaning only the local NHS staff responsible for care have access to personal identifying information.

No personal data will be leaving ESNEFT. Patients will be identified by their treating clinicians who are aware of their diagnoses and will list the patient hospital number in a password-protected spreadsheet. The list will be pseudo-anonymised by assigning a random number to the case, and anonymised data will be then gathered in the data collection tool. This ensures patient confidentiality. We will use two separate spreadsheets, one documenting the patient's hospital number and their assigned study number. This spreadsheet will not contain any other identifiable patient details (i.e. patient name, age, date of birth etc). A separate spreadsheet will contain patient study numbers only with medical history information relevant to the study. Both will be password protected secured on the NHS site. All data will be entered promptly and frequently cleaned.

The patient electronic patient records will be mined for information regarding age at onset, symptoms at onset, developmental issues, ongoing clinical history- recorded as Human Phenotype Ontology terms, diagnostic tests, duration of time till diagnostic tests such as electroencephalography in sleep or genetic tests undertaken, and duration of time till neuropsychology assessments (if any) undertaken. We will also record the underlying cause for ESES (where available), whether the patient has been discharged from ongoing follow-up and if there are ongoing physical or neuropsychological issues, at their current age. This information will be collected using a data collection tool, which will be an excel spreadsheet.

The anonymised dataset will be analysed by the research team. We will involve patient and family groups in the review of documents prior to dissemination of research findings.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Any Paediatric patient (up to 16 years old) who has been managed for electrical status epilepticus in sleep or developmental and/or epileptic encephalopathy with spike-wave activation in sleep, by clinicians at East Suffolk and North Essex NHS Foundation Trust, within the last 15 years.
  • Patients meeting criteria 1) with available electronic health records.

Exclusion criteria

  • Any Paediatric patient (up to 16 years old) with epilepsy managed by clinicians at East Suffolk and North Essex NHS Foundation Trust, where the diagnosis of electrical status epilepticus in sleep or developmental and/or epileptic encephalopathy with spike-wave activation in sleep was not confirmed.
  • Patients without electronic health record availability.
  • Patients over 16 years old.
  • Patients who have opted out of data use as per national opt out policy.

Treatment and study plan

Primary outcomes

  1. Creation of an evidence-based guideline

    Time frame: Over the past 10-15 years

    The primary outcome measure for the study is the creation of an evidence-based guideline using clinical experience of managing patients with electrical status epilepticus in sleep.

Secondary outcomes

  1. Diagnosis criteria

    Time frame: Over the last 10-15 years

    Diagnostic criteria used when patients were given a diagnosis of electrical status epilepticus in sleep (ESES)

  2. Treatments used

    Time frame: Over the last 10-15 years

    Treatments used prior to and after diagnosis of ESES

  3. Treatment response monitoring

    Time frame: Over the last 10-15 years

    How treatment response was monitored

  4. Duration of time

    Time frame: Over the last 10-15 years

    Duration of time taken to assess a patient using electroencephalography and neuropsychological tests

  5. Long term outcomes and clinical spectrum

    Time frame: Over the last 10-15 years

    Long term outcomes and clinical spectrum associated with ESES

Study contacts

Contact information is provided by the study sponsor or research team.

Thiloka Ratnaike

CONTACT

R&[email protected]

01473 704343

Sponsors and collaborators

Lead sponsor

East Suffolk and North Essex NHS Foundation Trust

Other

Registry information

Official study title

Study to Understand the Diagnostic Measures, Management Options and Long Term Outcomes in a Local Cohort of Patients with Electrical Status Epilepticus in Sleep, Also Known As a Developmental And/or Epileptic Encephalopathy with Spike-Wave Activation in Sleep

Acronym: SPESES

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jan 24, 2025
Registry last updated
Jan 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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