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Personalized Spine Study Group (PSSG) Registry

Personalized Spine Study Group (PSSG) Registry of Patients With Personalized Spine Rod Implantation

Who can join

Ages 10 to 85 · All sexes

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

About the study

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.

What is being tested

• Patient Specific Rod (device)

Sponsor: University of Colorado, Denver · Participants: 1,000 · Started: Oct 29, 2020

Contact the study team

• Christopher Kleck, MD · Phone: 720-848-1900
• jiandong hao · Phone: 303-724-7457

Official record on ClinicalTrials.gov — NCT04601363

Locations in the U.S.

Conditions

• Scoliosis
• Intervertebral Disc Degeneration
• Spinal Stenosis

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.