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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04716530
Other study ID # Istanbul MU CP
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 15, 2021
Est. completion date February 20, 2021

Study information

Verified date January 2021
Source Istanbul Medeniyet University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study will be carried of scanning the database of 296 individuals with cerebral palsy followed in the university pediatric rehabilitation clinic. Cerebral palsy risk factors and demographic information will be obtained from the database. The data will be classified according to date of birth, divided into 3 groups: those born before 2000, those born between 2000-2010, and those born after 2010.Changes in cerebral palsy risk factors will be investigated at 10-year intervals.


Description:

The study will be carried of scanning the database of 296 individuals with cerebral palsy followed in the university pediatric rehabilitation clinic. Cerebral palsy risk factors and demographic information will be obtained from the database. Cerebral palsy subtypes classified according to The Surveillance for Cerebral Palsy in Europe (SCPE) classification into four groups: spastic (unilateral and bilateral), dyskinetic (dystonic and choreoathetoic), ataxic/hypotonic, non-classifiable. Cerebral palsy risk factors will be primarily divided into 4 as preconceptional, antenatal, intrapartum and neonatal risk factors. Then, risk factors in the data will be distributed to the appropriate risk factor group. The data will be classified according to date of birth, divided into 3 groups: those born before 2000, those born between 2000-2010, and those born after 2010. Changes in cerebral palsy risk factors will be investigated at 10-year intervals.


Recruitment information / eligibility

Status Recruiting
Enrollment 296
Est. completion date February 20, 2021
Est. primary completion date January 30, 2021
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - cerebral palsy patients Exclusion Criteria: - missing data on the cerebral palsy database

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No intervention is associated with the study.
No intervention is associated with the study.

Locations

Country Name City State
Turkey Istanbul Medeniyet University Faculty of Medicine, Physical Medicine and Rehabilitation Department Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Istanbul Medeniyet University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Define the risk factors of cerebral palsy Risk factors of cerebral palsy questioned as preconceptional, antenatal, intrapartum and neonatal. 1 month
Primary Define the change in the risk factors among age groups The difference in cerebral palsy risk factors in age groups measured by chi-square statistics (born before 2000/ born between 2000-2010/ born after 2010) 1 month
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