Cerebral Palsy Clinical Registry Study Summary
Status: Active Timeline: March 2016 –
Study Type: Clinical Registry
The Cerebral Palsy Clinical Registry is a database of patient characteristics, interventions and outcomes for people with CP seen at participating centers in the CP Research Network. The CP Registry is used to provide preliminary data for research studies, aid in study design, and observe practice variation in the treatment of people with CP.
Study overview page: Cerebral Palsy Clinical Registry Overview
Inclusion criteria: Anyone with a diagnosis of CP seen at a CP Research Network center.
Exclusion criteria: Anyone with a progressive movement disorder that appears like CP and certain genetic conditions.
Principal Investigator(s): Garey Noritz, MD, Paul Gross
Study Contact: firstname.lastname@example.org