Rett Syndrome Registry (RSR)

  • STATUS
    Recruiting
  • End date
    Jul 30, 2028
  • participants needed
    3000
  • sponsor
    International Rett Syndrome Foundation
Updated on 5 August 2022
Investigator
Dominique C. Pichard, MD
Primary Contact
Gillette Children's Specialty Healthcare (4.6 mi away) Contact
+13 other location

Summary

The Rett Syndrome Registry is a longitudinal observational study of individuals with MECP2 mutations and a diagnosis of Rett syndrome. Designed together with the IRSF Rett Syndrome Center of Excellence Network medical directors, this study collects data on the signs and symptoms of Rett syndrome as reported by the Rett syndrome experts and by the caregivers of individuals with Rett syndrome. This study will be used to develop consensus based guidelines for the care of your loved ones with Rett syndrome and to facilitate the development of better clinical trials and other aspects of the drug development path for Rett syndrome.

Description


Details
Condition Rett Syndrome, Rett Syndrome, Atypical, Genetic Disease, Genetic Diseases, X-Linked, Intellectual Disability, Neurobehavioral Manifestations, Neurologic Manifestations, Neurologic Disorder, Neurodevelopmental Disorders, Nervous System Diseases
Clinical Study IdentifierNCT05432349
SponsorInternational Rett Syndrome Foundation
Last Modified on5 August 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Male or female with a pathologic loss of function alteration of MECP2

Exclusion Criteria

Male or female with a gain of function alteration of MECP2, including those with MEPC2 duplication or triplication
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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