Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
51 participants
OBSERVATIONAL
2018-01-02
2019-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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posterior surgery for spinal arthrodesis
posterior surgery for spinal arthrodesis
Eligibility Criteria
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Inclusion Criteria
* idiopathic scoliosis
* posterior surgery for spinal arthrodesis
* non opposition children and parents
Exclusion Criteria
* secondary intervention
* anterior surgery
* non idiopathic scoliosis
10 Years
18 Years
ALL
No
Sponsors
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Rennes University Hospital
OTHER
Responsible Party
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Principal Investigators
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Anne DEFONTAINE, MD
Role: PRINCIPAL_INVESTIGATOR
Rennes University Hospital
Locations
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CHU de Rennes
Rennes, , France
Countries
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Other Identifiers
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35RC17_3088_RACHIDOL
Identifier Type: -
Identifier Source: org_study_id
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