Image

Lorraine Registry of Multiple Sclerosis

Lorraine Registry of Multiple Sclerosis

Recruiting
All
Phase N/A

Powered by AI

Overview

The RelSEP aims to register exhaustively every new case of multiple sclerosis (MS) occuring in Lorraine a French region, and follow up on them for an indefinite duration, registering disease evolution and intercurrent events.

Description

As every patient registry in France, the RelSEP is periodically (every four years) evaluated by an independent committee.

The RelSEP interrogate multiple sources to insure its exhaustiveness :

  • every neurologists of Lorraine
  • MS patient network in Lorraine
  • health insurance data
  • PMSI (administrative French national database for hospitals)
  • biological and imagery services in Lorraine Procedures (automatic and manual) are used to eliminate duplicates Once a patient has been identified its medical file are checked by investigators in order to retrieve the relevant information.

New MS cases are confirmed by neurologists. Automatics (implemented in EDMUS software)and manual checks are implemented in the registry database, looking for inconsistencies.

The following data are registered :

  • Name, birthname
  • Sex
  • Date of birth
  • Location (town)
  • Birth location (town)
  • Profession
  • Number of siblings
  • Marital status
  • Number of children
  • Date of onset
  • Date and nature of clinical manifestations
  • MRI reports
  • CSF analysis reports
  • Event-related potential reports
  • Impairment and disability evolution
  • Treatments (start and change of drug treatment)
  • Drugs related events
  • Cause of treatment discontinuation
  • Disease progression Every case has a follow up at least every two years.

The quality of data is evaluated by periodically auditing cases at random from our database.

An annual report on the main data (incidence and prevalence) of MS in Lorraine is produced.

Data are also used for observational studies on prognostic factors.

Eligibility

Inclusion Criteria:

  • Having a confirmed multiple sclerosis diagnosis
  • Living in Lorraine (French region)

Exclusion Criteria:

  • Refusal to be registered

Study details
    Multiple Sclerosis

NCT02883335

Central Hospital, Nancy, France

28 January 2024

Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.