A Comparative Study of Hijamah Bila (Shurt Dry Cupping) Vs Habbe Asgand in the Management of Waja-uz-Zahr (Low Back Pain) An Open Label Randomized Controlled Clinical Trial
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Reduction of Oswestry Low Back Pain Scale
研究概览
简要总结
Enrolled cases of Waja-uz-Zahr (Low Back Pain) fulfilling the inclusion criteria after obtaining a written informed consent will be randomly allocated into group A and group B, each group contains 30 patients. Randomization will be done by lottery method. Patients of Group A will be treated with Hijamah-bila-Shurt (Dry Cupping) on every alternate day up to 14 days i.e. 0, 2nd, 4th, 6th, 8th, 10th, 12th, and 14th day. Total number of 8 sitting of Hijamah-Bila-Shurt will be given to the patients of Group A.
Patients of Group B will receive Habbe Asgand two pills (each 650mg) twice a day after meal for 14 days.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 20.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Clinically and radiologically diagnosed patients of Low Back Pain.
- •Willingness to participate in the study and give written consent.
排除标准
- •History of any major trauma.
- •History of any major systemic illness like diabetes mellitus, hypertension, CVD, CVA etc.
- •Pregnant and lactating women.
- •Prolapsed of intervertebral disc.
- •Low back pain secondary to a malignant or autoimmune disease.
- •Congenital deformities of the spine (except lordosis) Any skin disorders.
结局指标
主要结局
Reduction of Oswestry Low Back Pain Scale
时间窗: at baseline i.e. 00th day (Visit 1) , 7th (Visit 2) and 14th day (Visit 3)
次要结局
- Reduction of Visual Analogue Scale(at baseline i.e. 00th day (Visit 1) , 7th (Visit 2) and 14th day (Visit 3))
研究者
Shahid Amam
Government Tibbi College and hospital