A Study of Precice Intramedullary Limb Lengthening System (IMLL) Limb Lengthening Procedures

Enrolling by invitation

Conditions studied: Limb Length Discrepancy

In brief

The Sponsor is conducting a survey to understand how parents or legal guardians feel about the benefits of using the Precice IMLL System to lengthen limbs in children who are 12 years old or younger.

Key facts

Study ID

NCT06741514

Run by

NuVasive

People needed

100

Starts

2024-03-25

Expected to finish

2026-12-30

Last updated by the study team

2025-12-18

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• To be eligible for inclusion in this perceived clinical benefit survey study, the following inclusion criteria must be met:
• Participants must be a parent or legal guardian of a subject already enrolled in the Precice IMLL arm of the study, "A Retrospective Review of the Clinical and Radiographic Outcomes Following the Use of the Precice Intramedullary Limb Lengthening System (IMLL) in Pediatric Limb Lengthening Procedures" (NUVA.IMLL0723).
• The parent or legal guardian must be familiar with the patient's preoperative and postoperative condition, surgical treatment, postoperative care, and clinical outcomes.
• Informed consent from the parent or legal guardian of the patient is required for participation.

You may not qualify if…

• There are no exclusion criteria.

Where it is running

• Paley Orthopedic and Spine Institute — West Palm Beach, Florida, United States
• Nationwide Childrens Hospital — Columbus, Ohio, United States

Full record on ClinicalTrials.gov

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