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Study identifier: NCT07079865 Synced from ClinicalTrials.gov · July 30, 2026
● Recruiting

Effect of 60-day Peripheral Nerve Stimulation (PNS) in Alleviating Pain and Improving Function After Acute Thoracolumbar Compression Fracture

Condition: Thoracolumbar Compression Fractures  ·  Sponsor: Saint Peters University Hospital

PhaseN/A
Planned participants15
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

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Contact details are listed per location below or on the registry record.

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Locations (4)

University Orthopaedic Associates - Division of OrthoNJAvenel, New Jersey, United StatesRecruiting
University Orthopaedic Associates - Division of OrthoNJMorganville, New Jersey, United StatesRecruiting
University Center for Ambulatory Surgery (UCAS)Somerset, New Jersey, United StatesRecruiting
University Orthopaedic Associates - Division of OrthoNJSomerset, New Jersey, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07079865