跳至主要内容
临床试验/CTRI/2020/02/023639
CTRI/2020/02/023639尚未招募3 期

Clinical Validation of Unani Pharmacopoeial Formulation Laooq-e- Zeequn Nafas in Zeequn Nafas (Bronchial Asthma)

Central Council for Research in Unani Medicine CCRUM New Delhi0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方

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.Males and females of 18-65 years.
  • 2.Patients of Bronchial Asthma for at least 6 months presenting with at least one of the following symptoms:
  • b.Shortness of breath
  • c.Chest tightness and cough that vary over time and in intensity,
  • d.Expiratory airflow limitation as suggested by
  • a decreased FEV1
  • 3.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.
  • 4.Patients with Asthma Control Questionnaire Score > 1.5.

排除标准

  • 1.FEV1/FVC ratio < 50%
  • 2.Pregnant and lactating mother
  • 3.Patient with other Respiratory Tract Infections, tuberculosis and malignancy.
  • 4.Patient of Presence of chronic cough with expectoration for 2-3 months in each of 2 successive years.
  • 5.Patient with co-morbidities, Diabetes Mellitus, Hepatic and Renal Insufficiency.
  • 6.Patients with Tobacco Smoking.
  • 7.Patient with regular use of oral or systemic corticosteroids for conditions other than Asthma.

研究者

发起方
Central Council for Research in Unani Medicine CCRUM New Delhi

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