CTRI/2023/01/048733尚未招募2 期
A single blind, Randomized, Parallel Group study to compare efficacy and safety of Unani formulation Safoof-e-Dama Haldiwala with Salbutamol in patients with Zeequn Nafas(Bronchial Asthma)
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •(1) Patients of Bronchial Asthama for atleast 6 months having following symptoms: wheeze, Shortness of Breath, Chest Tightness and cough that vary over time and in intensity, Expiratory airflow limitation as suggested by a decreased FEV1.
- •(2) Objective evidence for reversible airway obstruction (>=12% and >=200 mL change in FEV1 and/or a 25% and 60 L/min change in PEFR) either spontaneously or after treatment.
- •(3) patients with Asthma Control Questionnaire Score >1.5
排除标准
- •The patients of Zeeq-un-Nafas (Bronchial Asthma) with following conditions will be excluded from the study:
- •1. Patients below 18 years and above 65 years of age., 2. Pregnant and lactating mother
- •3. FEV1/FVC ratio < 50%
- •4. Patient with other Respiratory Tract Infections, tuberculosis and malignancy.
- •5. Patients with Presence of chronic cough with expectoration for 2-3 months in each of 2 successive years.
- •6. Patient with co-morbidities, Diabetes Mellitus, Hepatic, Renal Insufficiency and Heart disease .
- •7. Patients with Tobacco Smoking.
- •8. Patient with regular use of oral or systemic corticosteroids for conditions other than Asthma.
研究者
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