Clin2
NCT07020000Possibly a fitRecruiting

Lumbar fusion with EARP nerve cuff electrode

Transforaminal Lumbar Interbody Fusion Surgery

Part of Bones, joints & muscles, Brain & nervous system, Pain clinical trials.

This trial uses a medical device called the EARP Interbody System with a nerve cuff electrode during lower back fusion surgery. It collects real-world data to confirm the device is safe and works well for people having fusion between the second and fifth lumbar vertebrae.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
120 people
Ages
22 years to 80 years
Study type
Observational

Who can take part

  • You are having lower back fusion surgery involving the L2 to S1 vertebrae.
  • Your body mass index (BMI) is 40 or lower.
  • You are not pregnant and do not plan to become pregnant soon.
  • Your surgery will only use the EARP device, not a combination with other fusion techniques.
  • You do not have certain spine conditions like non-healed prior fusion, severe spondylolisthesis, vertebral compression fractures, spinal metastasis, or acute spine trauma.
  • You do not have allergies to the device materials (titanium, platinum, PEEK, aluminum, stainless steel, or silicone).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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