KCT0003321已完成未知
Comparison of Pain score and Treatment effect between Bolus infusion method and Continuous infusion method when Hypertonic saline infusion in epidural adhesiolysis
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 18(Year) 至 80(Year)(—)
- 性别
- All
入选标准
- •(1) patients between 18 and 80 years of age; (2) patients with a history of chronic low back pain and/or lower extremity radiating pain of at least 6 months; (3) patients who received lumbar epidural adhesiolysis with a 1-day protocol including hypertonic saline infusion; (4) patients with numerical rating scale (NRS) pain scores of 6 or more after appropriate conservative treatments, such as oral analgesics, physical therapy and epidural steroid injection.
排除标准
- •(1) complaints of back pain more severe than leg pain; (2) lack of correlation between neuropathic back pain with radicular symptoms and MRI findings; (3) lumbar surgical intervention in previous 6 months; (4) coagulopathy, chronic infection or skin infection at the procedure site; (5) poorly controlled psychiatric disorders or acute medical illness, underlying systemic diseases that could interfere with the interpretation of the outcome assessments; (6) pregnant or lactating women; (7) with a history of adverse reaction to local anesthetics or steroids; (8) patients who require other interventions with uncontrolled pain during the follow-up period; (9) patients unable to understand the informed consent and protocol and (10) patients unable to be positioned in prone position to perform the procedure.
研究者
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