A randomized Comparative clinical trial on the efficacy of Dalk Mutadil (moderate massage) with Rogan-e-Baboona vs. Hijama bila shart (cupping without scarification) in frozen shoulder.
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 34
- 试验地点
- 1
- 主要终点
- Improvement in Quality of life - Shoulder pain and disability
研究概览
简要总结
A randomized comparative clinical trial on the efficacy of Dalk Mu’tadil (moderate massage) with Rogan-e-Babunah vs. Hijama bila shart (cupping without scarification) in frozen shoulder.
Duration : 20 days
Sample Size : 30
IEC No: GUMC/IEC/2022-2023/MJ/23/06
Out Comes:
Primary Outcome: Improvement in AROM (Goniometer). Improvement in Quality of life - Shoulder pain and disability index scale (SPADI).
Secondary Outcome: Relief in Pain Visual Analogue Scale (VAS).
Objective of the Study: To assess the clinical efficacy of Dalk Mu‘tadil with Roghan-e-Babunah and ḤijÄma bilÄ Shará¹ in Frozen shoulder patients.
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
- 40.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients of all genders will be selected for the study.
- •Age between 40 to 60 years.
- •Painful and difficult (unilateral or bilateral) shoulder mobility.
- •The duration of the symptoms exceeds four months.
- •Frozen Shoulder cases with a clinical diagnosis.
排除标准
- •Patients below 40 and above 60 years of age.
- •Pregnant and lactating mothers.
- •H/O Shoulder injury and surgery, local corticosteroid injections within the previous four months, or current corticosteroid medication.
- •Patients who fail to give consent.
- •Fracture or dislocation of the affected shoulder.
- •A history of any systemic, metabolic, or infectious diseases.
结局指标
主要结局
Improvement in Quality of life - Shoulder pain and disability
时间窗: 20 days
index scale (SPADI).
时间窗: 20 days
Relief in Pain Visual Analogue Scale (VAS)
时间窗: 20 days
次要结局
- improvement in quality of life (SPADI)(20 days)
研究者
Dr Mohammed Waseem
Government Unani Medical College, Chennai