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.
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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