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Search / Trial NCT04540068

Prediction of TEI Success in Sciatica

Launched by EDUARD VERHEIJEN · Sep 1, 2020

Trial Information

Current as of July 22, 2025

Recruiting

Keywords

Transforaminal Epidural Injection Lumbar Spine Prospective Cohort Study Prediction Of Success

ClinConnect Summary

This clinical trial, titled "Prediction of TEI Success in Sciatica," is studying how well a common treatment called transforaminal epidural injection (TEI) works for patients suffering from specific back conditions like lumbar radiculopathy, which is often caused by issues like herniated discs or spinal stenosis. The goal is to figure out which patients are most likely to benefit from this treatment based on their individual characteristics, such as age, medical history, and imaging results. Researchers will also look at how effective the treatment is in reducing pain and improving daily activities in the short term, as well as any side effects that might occur.

To be eligible for this trial, participants need to be adults aged 18 and older who have been diagnosed with a specific type of back pain related to lumbar radiculopathy, confirmed by an MRI. They should also be scheduled for a TEI. Those with certain complications or previous treatments that could interfere with the study won't be included. If you join the trial, you can expect to have your pain and functionality assessed at various points after the treatment, helping researchers understand how well TEI works for different patients. Overall, this study aims to improve treatment outcomes for individuals facing similar back issues.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Diagnosis of unilateral lumbar radiculopathy secondary to LDH or one-level spinal stenosis
  • Diagnosis supported by magnetic resonance imaging (MRI) findings
  • Scheduled appointment for TEI
  • Access to e-mail
  • Signed informed consent
  • Exclusion Criteria:
  • Diagnosis of unilateral lumbar radiculopathy secondary to LDH or one-level spinal stenosis
  • Age under 18 years
  • Severe multisegmental spinal disease
  • Anatomical abnormalities that may complicate the procedure technically (e.g. severe scoliosis)
  • Active malignancy or infectious disease
  • Use of immunosuppressive drugs
  • Use of systemic corticosteroids in preceding 3 months
  • Previous treatment with TEI for current episode of lumbar radiculopathy
  • History of lower back surgery at the same lumbar level
  • Circumstances that prevent treatment with TEI (e.g. use of anticoagulants that cannot be temporarily discontinued, allergy against steroids or local anaesthetic)
  • Pregnancy
  • Major language barrier

About Eduard Verheijen

Eduard Verheijen is a dedicated clinical trial sponsor with a strong commitment to advancing medical research and improving patient outcomes. With a focus on innovative therapies and rigorous trial methodologies, Verheijen leads initiatives that prioritize ethical standards and regulatory compliance. His expertise encompasses a wide range of therapeutic areas, fostering collaborations with research institutions and healthcare professionals to ensure the successful execution of clinical studies. By leveraging cutting-edge technology and data-driven approaches, Eduard Verheijen aims to enhance the efficiency and effectiveness of clinical trials, ultimately contributing to the development of groundbreaking treatments.

Locations

Haarlem, , Netherlands

Patients applied

0 patients applied

Trial Officials

Carmen LA Vleggeert-Lankamp, MD, PhD

Principal Investigator

Leiden University Medical Centre / Spaarne Gasthuis

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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