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Completed

NCT Number: NCT03353194

Canadian CP Registry - Registre Canadien de la Paralysie Cérébrale

The Canadian Cerebral Palsy (CP) Registry is a confidential, nation-wide collection of medical and social information about children with cerebral palsy. The Registry was first implemented in 2003 in 6 administrative regions of Quebec and was later extended to paediatric centres in Newfoundland, Nova Scotia, Ontario, Alberta, and British Columbia. Over 1850 children living with Cerebral Palsy have been registered so far. The Registry is the first national registry for cerebral palsy in North America.

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Key information

Age range

18 month–18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Alberta Children's Hospital, Calgary, Alberta, Canada

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About this study

The Canadian Cerebral Palsy Registry is a multi-regional Canadian registry to identify potential risk factors related to pregnancy and interactions of the environment and genetics. The Registry provides researchers with the approximate number of children with cerebral palsy across Canada, and data in the Registry helps researchers explore reasons behind the causes of cerebral palsy, in addition to supporting studies which may lead to improvements in the overall care of children with CP.

Cerebral palsy is the most common cause of physical disability in children in Canada and it is important that we gain a better understanding of its prevalence, risk factors and current clinical profile. The Canadian CP Registry provides valuable data from different Canadian regions which can be shared and analyzed so as to provide answers to these important questions. Specifically, the Registry serves to:

  • Characterize the profile of children living with CP across the country
  • Identify risk factors associated with CP
  • Monitor the prevalence of CP across the country
  • Provide a platform for subject recruitment for population-based research on CP

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Under 18 (age cut-off varies by region)
  • Diagnosed with Cerebral Palsy
  • Living in Canada

Exclusion criteria

  • Uncertain CP diagnosis

Treatment and study plan

Primary outcomes

  1. Characterize the CP profile across Canada

    Time frame: An average of every two years, up to study completion or ten years, whichever comes first.

    CP subtype, severity, and associated conditions

Sponsors and collaborators

Lead sponsor

McGill University Health Centre/Research Institute of the McGill University Health Centre

Other

Collaborators

  • Alberta Children's Hospital
  • Children's Treatment Network
  • Holland Bloorview Kids Rehabilitation Hospital
  • IWK Health Centre
  • Kids Brain Health Network
  • Montreal Children's Hospital of the MUHC
  • Provincial Health Services Authority British Columbia
  • The Hospital for Sick Children
  • Women and Children's Health Research Institute, Canada

Registry information

Official study title

The Canadian Cerebral Palsy Registry - Le Registre Canadien de la Paralysie Cérébrale

Important dates

Study start
2004
Primary completion
2020
Study completion
2020
First posted
Nov 27, 2017
Registry last updated
Feb 25, 2021

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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