CTRI/2023/01/049134尚未招募不适用
A randomized single blind multi-arm study for comparative therapeutic evaluation of plain and medicated bukhoor (plain and medicated vapour therapy)in the management of non specific low back pain
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 120
- 试验地点
- 1
- 主要终点
- VAS
研究概览
简要总结
| Background: Low Back pain especially Non-specific low back pain is very prevalent so we need to find effective alternative treatments having minimal side effects. |
Purpose: The purpose of the trial is to find the safe and effective treatment of Non-specific low back pain outside pharmacotherapy.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 50.00 Year(s)（—）
- 性别
- All
入选标准
- •Clinically diagnosed patients with low back pain as the chief complaint.
- •characterized by intermittent, recurrent, and episodic problems; and includes four types of pain: local, referred, radicular, and that arising from secondary(protective) muscular spasm.
- •Lower back pain persisting for 4 weeks or more.
- •Patients of either gender.
- •Age bracket 18-50 years.
- •Patient willing to abide for protocol guidelines.
排除标准
- •Age below 18 years and above 50 years.
- •Recent low back injury.
- •Pregnant and lactating women.
- •Any specific pathology.
结局指标
主要结局
VAS
时间窗: 30 days.
Improvement in :
时间窗: 30 days.
Sign symptoms
时间窗: 30 days.
Oswestry low back pain disability scale
时间窗: 30 days.
SF-12
时间窗: 30 days.
Mc Gill Pain Questionnaire.
时间窗: 30 days.
次要结局
- ELISA(OSI(Oxidative stress index))
研究者
研究点 (1)
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