Menu
Recruiting NCT02821260

Clinical Evaluation of the Efficacity of Epilepsy Surgery in Infants and Children

Observational Epilepsy

For patients and families

In plain language

Fill the application

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Epilepsy. Basic parameters: up to 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The Pediatric Neurosurgery Service of the Rothschild Foundation (Paris) is the French leader center for surgery of epilepsy in infants and children. Postoperative follow-up of these children is performed during medical and neurosurgical consultations in order to assess the frequency of attacks and to reduce medication. On average, two postoperative consultations are carried out between 3 and 5 months and between 12 and 18 months. Beyond 18 months, some children may benefit from long-term monitoring at this center, but most children are followed by their neurologist . Therefore, the center has no rigorous and systematic collection of standardized data on the outcome of these patients. The purpose of this study is to evaluate the efficacy of the epilepsy surgery in children with a monitoring of 3 years.

Primary outcome measures

  • Number of seizures [Time frame: Three years]

Eligibility criteria

Inclusion criteria

  • Child treated surgically for epilepsy at the Rothschild Foundation (Paris, France)

Exclusion criteria

  • Parental opposition to the participation of their child to the study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

France · 1 center
  • Fondation Ophtalmologique Adolphe de Rothschild — Paris

Identifiers

NCT: NCT02821260 · CBU_2015_29

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗