Effect of 60-day Peripheral Nerve Stimulation (PNS) in Alleviating Pain and Improving Function After Acute Thoracolumbar Compression Fracture
Start Date
8/7/2025
Completion Date
12/1/2026
Summary
The purpose of this study is to track and investigate the outcomes of female patients with acute thoracolumbar compression fractures, focusing on pain management and functional improvement. The study will investigate patients whose compression fractures are within 3 months or less and measure pain scores, using the Numeric Rating Scale (NRS) and Brief Pain Inventory (BPI) and quality of life using the PROMIS questionnaire at 1-week prior to intervention and then 2 weeks, 3 months and 6 months post PNS implantation. The primary aim is to assess pain reduction among participants that receive the 60-day PNS intervention. The secondary aim is to analyze functional outcomes and quality of life documented in PROMs (Patient Reported Outcomes Measures) provided by CareSense a digital data collection system.
Eligibility Criteria
Age Range: 18 years to No maximum
Interventions
SPRINT PNS modulation system
Conditions
Locations
University Orthopaedic Associates - Division of OrthoNJ
Avenel, New Jersey 07001
United States
University Orthopaedic Associates - Division of OrthoNJ
Morganville, New Jersey 07751
United States
University Center for Ambulatory Surgery (UCAS)
Somerset, New Jersey 08873
United States
University Orthopaedic Associates - Division of OrthoNJ
Somerset, New Jersey 08873
United States