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NCT05544058Completed

Retrospective Non-interventional Study of Stiripentol Use in Dravet Patients in the USA

Source: ClinicalTrials.gov · Last updated 2 Aug 2024

Brief summary (registry, in English)

The present study aims to collect data regarding the history of the disease, previous and current treatments, and the clinical status of Dravet patients during the 3 months prior to stiripentol initiation, the first 3 months on stiripentol and the last 3 months on stiripentol (irrespective of stiripentol discontinuation).

Status (registry)
Completed
Study type
Observational
Enrollment
100 (actual)
First submitted
24 Aug 2022
Start date
27 Apr 2022
Primary completion date
28 Jun 2024
Lead sponsor
Biocodex
Diseases
Epilepsy
NCT number
NCT05544058

What you commit to

  • Study type: Observational
  • Participants enrolled: 100
  • From 27 Apr 2022 to the primary completion date, 28 Jun 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • NA

Who the study is looking for

  • Patients diagnosed with Dravet syndrome
  • Treated with stiripentol for a minimum of 3 months in routine practice

Sex: All

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mayo Clinic
Coordinator of this site? Confirm its status
RochesterUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.