CTRI/2021/09/036532尚未招募不适用
A Clinical Study on Warm-e Tajaweef-e-Anf-Muzmin (Chronic Rhinosinusitis) and Comparative Evaluation of Unani Formulations in its Management:A Randomized,single blind parallel Group comparative study
Department of moalejat Ajmal khan tibbiya college and hospital Aligarh muslim university1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2021年9月20日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Improvement in clinical features
研究概览
简要总结
A clinical study on waram-e-tajaweef anf muzmin (chronic rhinosinusitis and comparative evaluation of unani formulations (qurs e musakkin and mufeed joshanda) in its management
研究设计
- 研究类型
- Interventional
- 分配方式
- Random Number Table
- 盲法
- Open Label
入排标准
- 年龄范围
- 15.00 Year(s) 至 50.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients fulfilling AAO-HNS criteria that is atleast two major criteria (Nasal obstruction or blockage ,anterior or posterior nasal discharge ,Facial pain /congestion , Purulence in nasal cavity on examination ,Anosmia/ Hyposmia ) or one major and two minor criteria (Halitosis , earache, dental pain , cough , fatigue) patients having opacity of Xray paranasal sinuses ( water’s view )ranging from +1 (Mucosal thickening )to +3 (complete opaque antrum) grading.
- •Patients of either sexes.
- •Patients in the age group of 15 to 50 years.
- •Patients with involvement of any sinus.
- •Those who give written consent.
排除标准
- •1.Children below 15 years of age.
- •Pregnant & lactating mothers.
- •4.Patients who fail to give consent.
- •6.Mentally retarded persons.
- •7.Patients with Malignancy of the nose or paranasal sinuses.
- •8.Patients having history of any surgery of nose or paranasal sinuses.
- •10.Patient having history of trauma to nose or sinus areas.
- •11.Patients suffering from any congenital or acquired structural abnormality of the nasal cavity.
- •12.Any medical condition where physician feels that participation in the study could be detrimental to patient’s well being.
- •13.Patients of pulmonary koch’s or patient having history of epistaxis.
结局指标
主要结局
Improvement in clinical features
时间窗: Weekly for 6 weeks
次要结局
- Changes in the X-ray PNS waters view with the help of an arbitrary scale(At start of the intervention and at the end of the 6 week)
研究者
研究点 (1)
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