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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04761666
Other study ID # PI2021_843_0036
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date February 16, 2021
Est. completion date July 1, 2023

Study information

Verified date July 2023
Source Centre Hospitalier Universitaire, Amiens
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Low bone mineral density affects 77% of children with severe cerebral palsy (GMFCS IV & V) with an increased fracture risk of 4%. One strategy supposed to improve bone mineral density is verticalisation with static devices. Nowadays there is no time recommendation of verticalisation however high intensity verticalisation has been shown to be effective in improving bone mineral density in childrens with cerebral palsy, but difficult to apply in real life due to lack of qualified therapists, device's complexity, and severe impairment in those children. The investigators aim to compare bone mineral density and bone remodelling factors of verticalized and non verticalized childrens with severe cerebral palsy as achieved in everyday life. The investigators conduced a retrospective study comparing bone mineral density and factors who influence bone remolling in severe cerebral palsy's according to whether they are verticalized or not.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date July 1, 2023
Est. primary completion date July 1, 2023
Accepts healthy volunteers No
Gender All
Age group 3 Years to 18 Years
Eligibility Inclusion Criteria: - patients with cerebral palsy GMFCS (gross motor functional classification scale) IV-V - age of patients 3-18 years Exclusion Criteria: - patients with neuro muscular disease - patient age < 3 years old and > 18 years old - patient with constitutionnal bone disease - patient with growth hormone treatment - patient with surgery < 6 months - patient with fracture <3 months - Refusal of the legal representative

Study Design


Locations

Country Name City State
France CHU Amiens Amiens

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Variation of Densitometric Z score between both groups A Z-score compares the patient bone density to the average bone density of people your own age and gender.A Z-score is helpful in diagnosing secondary osteoporosis and is always used for children. It is most useful when the score is less than 2 standard deviations below this normal. In this setting, it is helpful to scrutinize for coexisting illnesses or treatments that may contribute to osteoporosis such as glucocorticoid therapy, hyperparathyroidism, or alcoholism. 6 months
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