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Swiss Cerebral Palsy Registry

Key facts

Who runs it
University of Bern
Where
Switzerland12 sites in 1 countryChoose a country to see its sites
Trial code
Status
Recruiting
People taking part
15,000 people, planned
Started
19 Jun 2017
Expected to end
Jan 2071
Type of study
Observational
Record updated
13 February 2026

Who can take part

Age
0 years and older
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 6 criteriaShow less

Who can take part

  • Who were diagnosed with CP, confirmation of the diagnosis at the age of 5 years is required
  • Who are born, treated for CP or living in Switzerland, and
  • Who gave informed consent

Who cannot take part

  • Neurometabolic diseases (e.g. neuronal storage diseases, leukodystrophies)
  • Other progressive neurological diseases (e.g. spinocerebellar ataxias, hereditary spastic paraplegia, Rett syndrome, epileptic encephalopathy)
  • Pure muscular hypotonia

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

About the trial

What the trial wants to find out

The Swiss-CP-Reg is a national patient registry that collects information on diagnosis, symptoms, treatment and follow-up of patients with cerebral palsy (CP) in Switzerland. It was first implemented in 2017 in the paediatric clinics in Basel, Bellinzona, Bern, Geneva, Lausanne, St. Gallen and Zurich. It is currently extended to all Swiss clinics and medical practices and adults will be invited to join the register in the coming years. The registry provides data for national and international monitoring and research. It supports research on CP in Switzerland and the exchange of knowledge between clinicians, researchers and therapists, with the goal to improve the treatment of children and adults with CP and optimizing their health and quality of life.

The group in the trial

  • Patient population

    Children, adolescents and adults diagnosed with cerebral palsy who are born, treated or living in Switzerland

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Record updated
13 February 2026