Personalized Spine Study Group (PSSG) Registry

Recruiting now

Conditions studied: Scoliosis; Adolescence, Degenerative Disc Disease, Spinal Fusion, Kyphoscoliosis, Pseudoarthrosis of Spine, Spinal Stenosis, Kyphoses, Scheuermann

In brief

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.

Key facts

Study ID

NCT04601363

Run by

University of Colorado, Denver

People needed

1000

Starts

2020-10-29

Expected to finish

2030-04-01

Last updated by the study team

2024-10-03

Who can join

Age: 10 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patient has been/ will be operated and instrumented with patient-specific rod or spine hardware (control cohort)
• Patient able to consent or assent

You may not qualify if…

• 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

Where it is running

• Dr. Christopher Kleck, MD — Aurora, Colorado, United States (enrolling)

Full record on ClinicalTrials.gov

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