跳至主要内容
临床试验/CTRI/2023/04/051441
CTRI/2023/04/051441尚未招募Unknown

A comparison on the efficacy of low volume versus high volume injection of epidural steroids in the management of back pain and radiculopathy associated with lumbar degenerative disc disease - A Randomised superiority clinical trial.

Government medical college Kozhikode0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
尚未招募

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Adult patients (aged 25-50 Years), capable of providing consent and complying with the outcome
  • instruments
  • 2. Single-level lumbar disc herniation diagnosed by MRI
  • 3. Lower lumbar disc herniation diagnosed by MRI (L4/L5 or L5S1).
  • 4. Signs and symptoms consistent with the nerve root irritation
  • 5. Patients with lumbar radicular pain, irrespective of neurological signs.
  • 6. Patients have refractory pain, even after treatment with NSAIDs, opioids, and/or physical
  • therapies for more than two weeks duration.
  • 7. Failure after a minimum of 6 weeks of conservative treatment

排除标准

  • Patientâ??s reluctance and lack of compliance, does not provide informed consent for the
  • 2. Patients with previous back surgery at the affected segmental level and radiologically
  • proven facet syndrome
  • 3. Multiple level lumbar disc herniation diagnosed by MRI
  • 4. Patients with a severe motor deficit, segmental instability, spinal deformities.
  • 5. Any systemic infection or local infection at the injection site
  • 6. Patients presenting with cauda equina syndrome
  • 7. Patients on anticoagulation therapy or having any bleeding disorder
  • 8. Patients with congestive heart failure or uncontrolled blood sugars
  • 9. Pregnant females or ongoing breastfeeding females
  • 10. Patients with underlying malignancy
  • 11. Patients are not excluded based on the duration of pain alone.
  • 12. Patients who are allergic to any component of the medicine?

研究者

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