Comparative Clinical Study to evaluate the effect of Panchakoladi Avleha and Tamakswasahara Avleha in the management of Bal Tamakaswasa w.s.r. to Childhood Asthma

Principal1 个研究点分布在 1 个国家目标入组 40 人开始时间: 2021年9月13日最近更新: 2022年2月15日

试验速览

阶段: 不适用
状态: 招募中
发起方: Principal
入组人数: 40
试验地点: 1
主要终点: Fulfillment of objective and subjective criteria.

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

Research Report will be soon published after the completion of trial. 40 patients fulfilling the inclusion and exclusion criteria will be randomly selected from the OPD and IPD of Department of Kaumarbhritya, RGGPG Ayurvedic College and Hospital, Paprola. Patients will be divided randomly into 2 groups; Group 1 and Group 2 each with 20 patients. Group 1 will be given Panchkoladi Avleha orally while group 2 will be given Tamakswasahara Avleha orally. Result will be assessed on the basis of subjective and objective assessment criterias.

研究设计

研究类型: Interventional
分配方式: Other
盲法: Open Label

入排标准

年龄范围: 5.00 Year(s) 至 16.00 Year(s)（—）
性别: All

入选标准

•Parents/guardians of the children willing to participate in research trial.
•Only mild to moderate stable patients of childhood asthma will be included.
•Positive test of reversibility in oxygen saturation, PEFR,FEV1:FVC in children.
•Age group between 5 to 16 years.

排除标准

•Parents/parents of the patients not willing to participate in research trial.
•Patients having severe childhood asthma/ Status asthamaticus condition.
•Patient presenting systemic illness like pneumonitis, pleural effusion, pulmonary TB etc.
•Children with congenital anomalies.
•Patient with PEFR<50% & FEV1<50%.
•Patient on prolonged (>6week) medication with corticosteroids, bronchodialators, mast cell stablizers,anticholinergics etc.

结局指标

主要结局

Fulfillment of objective and subjective criteria.

时间窗: 28 days

次要结局

General feeling of well-being(28 days)

研究者

发起方

Principal

申办方类型

Research institution and hospital

研究点 (1)

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