RecruitingNot Applicable

Personalized Spine Study Group (PSSG) Registry

United States1,000 participantsStarted 2020-10-29

Plain-language summary

The primary objective of the study is a data collection initiative. The study will collect clinical and radiographic outcomes of patients implanted with patient specific rods. The secondary objective is to collect clinical and radiographic outcomes of patients with hardware as a control cohort to the patient-specific rods.

Who can participate

Age range10 Years – 85 Years

SexALL

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

Inclusion Criteria: * Patient has been/ will be operated and instrumented with patient-specific rod or spine hardware (control cohort) * Patient able to consent or assent Exclusion Criteria: * Patient unable to sign an informed consent form * Patient unable to complete a self-administered questionnaire * Patient is pregnant or planning on becoming pregnant during the duration of their study participation * Patient is older than 85 * Patient is younger than 10

What they're measuring

Patient-Specific Hardware Spino-Pelvic Measurements

Timeframe: Up to 4 years

Trial details

NCT IDNCT04601363

SponsorUniversity of Colorado, Denver

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2030-04

Contact for this trial

Christopher Kleck, MD

720-848-1900 Christopher.Kleck@CUAnschutz.edu

View on ClinicalTrials.gov More Scoliosis; Adolescence trials