TerminatedNot Applicable

UNiD Rods Register

Stopped: Early terminated for administrative reasons

Belgium, France743 participantsStarted 2015-01

Plain-language summary

Retro-prospective study allowing inclusion of patients with spinal deformities treated by patient-specific rods (UNiD). This study aims to assess performance, clinical outcomes and safety

Who can participate

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patient operated with UNiD® Patient Specific rods from MEDICREA® INTERNATIONAL * Patient affiliated to health care insurance (social security in France) * Patient able to complete a self-administered questionnaire * Patient able to sign a disclosure form or a non-opposition form Exclusion Criteria: * Patient not operated with Patient Specific rods from MEDICREA® INTERNATIONAL * Pregnant patient * Patient not affiliated to health care insurance (social security in France) * Patient unable to sign a disclosure form * Patient unable to complete a self-administered questionnaire

What they're measuring

Radiological performance compared to planning

Timeframe: 12 months

Trial details

NCT IDNCT02926404

SponsorMedicrea International

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2022-10

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