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

Recruiting now

Conditions studied: Thoracolumbar Compression Fractures

In brief

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.

Key facts

Study ID: NCT07079865
Run by: Saint Peters University Hospital
People needed: 15
Starts: 2025-08-07
Expected to finish: 2026-12-01
Last updated by the study team: 2026-02-18

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

Adult females ages 18+
Osteoporosis diagnosis with acute/subacute insufficiency fractures of the thoracic or lumbar spine identified on MRI or X-ray with significant pain and activity limitation.
Onset of pain from associated fracture should be less than 3 months.
Minimum pain should be 4 or greater (Moderate) on the NRS scale and/or impairing their daily activity.
Patients reported pain should be despite OTC medication trials of NSAIDs, Tylenol, lidocaine patches or similar medications.
Patients may be taking opioids while receiving treatment however as per routine practice, no additional opioids will be prescribed during the PNS intervention.

You may not qualify if…

Patients with pathological fractures, other etiologies of fracture such as pagets disease, multiple myeloma, local or systemic infection, untreated coagulopathy, untreated psychosocial disease.
Other etiologies of osteoporosis other than primary osteoporosis will be excluded such as hyperparathyroidism, anorexia, malabsorption, hyperthyroidism, or overtreatment of hypothyroidism, chronic renal failure, cushing.
Patients with diminished mental capacity (mental condition that will inhibit their ability to complete the assessments) as determined by the investigator.
Patients with an active cardiac implant device such as a pacemaker or defibrillator.

Where it is running

University Orthopaedic Associates - Division of OrthoNJ — Avenel, New Jersey, United States (enrolling)
University Orthopaedic Associates - Division of OrthoNJ — Morganville, New Jersey, United States (enrolling)
University Center for Ambulatory Surgery (UCAS) — Somerset, New Jersey, United States (enrolling)
University Orthopaedic Associates - Division of OrthoNJ — Somerset, New Jersey, United States (enrolling)

Full record on ClinicalTrials.gov

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