Efficacy of Hijama Bila Shart in Wajaur Raqaba - A randomized clinical trial
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 45
- 试验地点
- 1
- 主要终点
- Reduction in pain
研究概览
简要总结
Cervical spondylosis is a degenerative condition of cervical spine in the general population, occurs mostly in 4th and 5th decades of life.Abouttwo third of the population have neck pain at some time in their live and prevalence is highest in middle age.As neck pain affectes persons life both at home and at work,therfore relief from pain is mandatory for social , psychological, economical and medical reasons.
In Unani system of medicine tje term Wajaur Raqaba is not mentioned in any clasiscal test books, but most of the eminent physicians have used a broad term Waja ul Mafasil to describe all types of joint pain. unani physicians have treated Waja ul Mafasil successfully with various drugs and regimenal modalities including hijamah bila shart, dalk, riyazat etc, hijamah bila shart is one which is commonly prescribed to evacuate Mawad e Fasida and provide relief to the patient of Waja ul mufasil. The main aim of the study is to optimize the duration of application of cups in the pain management of wajaur raqaba. Total duration of the study is 15 days ,inclusion criteria will be clinically and radiologically diagnosed patients of wajaur raqaba of 20 to 60 years of age of either gender. total 3 cups will be applied ,1 large cup over the junction of 7th cervical vertebra and 1st thoracic vertebra and 2 medium cups will be applied over the right and left supraclavicular fossa for 8,10,and 12 minutes respectively in each group .Total 15 patients will be there in each group.Any adverse reaction during therapy will be recorded and reported.The outcome will be assessed by using VAS scale and Vernon and Mior Cervical spine questionnaire.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Open Label
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 Wajaur Raqaba.
- •Age between 20 -60 years.
- •Either gender.
排除标准
- •History of cervical trauma or injury.
- •Concomitant skin infections, Tuberculosis and cancer at the level of cervical spine.
- •Any post healed cervical fracture.
- •All types of arthritis except osteoarthritis.
- •Increased kyphosis and lordosis.
- •Tumours (Benign or Malignant) at the level of cervical spine.
- •Any subject undergoing any systemic medical or surgical or physical therapy for cervical radiculopathy .
- •Corticosteroid use, including oral corticosteroid within 14 days, intramuscular corticosteroid within 30 days, Intra-articular corticosteroid into the study cervical region within 90 days, and ongoing use of topical corticosteroid at the site of application.
- •Cervical rib syndrome.
- •Unwillingness or inability to comply the requirements of the protocol.
结局指标
主要结局
Reduction in pain
时间窗: 0th day and 15th day
Visual Analogue Scale (VAS)
时间窗: 0th day and 15th day
次要结局
- Neck disability index(NDI)(0th day and 15th day)
