跳至主要内容
临床试验/CTRI/2025/04/086062
CTRI/2025/04/086062尚未招募2 期

AN OPEN LABELLED DOUBLE ARM NON RANDOMIZED PHASE II CLINICAL TRIAL TO EVALUATE THE EFFICACY OF SADAMANJIL CHOORANAM AND SADAMANJIL CHOORANAM WITH SIDDHAR YOGA MARUTHUVA MURAIGAL IN THE MANAGEMENT OF ERAIPPU (BRONCHIAL ASTHMA)

DR S SATHISH KUMAR1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年5月14日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
The study aims at bringing light on the Efficacy of the long standing traditional practice of Siddha Yogam Muraigal and Sadamanjil chooranam towards the management of Eraippu (Bronchial Asthma ).

研究概览

简要总结

It is an open labelled double arm non randomized phase II Clinical trial to evaluate the efficacy of,

A. INTERNAL MEDICATION

  1. SADAMANJIL CHOORANAM

Dosage: 1to 3 grams twice a day with Luke warm water after food administered to Group A containing 20 participants for a period of 48 Days

B. INTERNAL MEDICATION AND SIDDHAR YOGIC INTERVENTIONS

Synergistic effect of the INTERNAL MEDICATION Sadamanjil Chooranam along with SIDDHAR YOGIC INTERVENTIONS including Pranayamam, Tirikonasanam, Bhujangasanam, Ardha Machasanam and Savasanam to Group B containing 20 participants for a period of 48 days

The efficacy of treatment is monitored and assessed through peak flow meter.

研究设计

研究类型
Interventional
分配方式
Not Applicable
盲法
Not Applicable

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Breathlessness, Wheezing with unproductive cough, Chillness of limbs, Obstructive Sleep Apnea, Allergic Rhinitis, Sputum expelled with cough with dyspnea.

排除标准

  • Chronic Bronchitis, Pulmonary Tuberculosis, Sinusitis, Interstitial Lung disease, Bronchiectasis, Any other serious systemic illness, Pregnancy and Lactation.

结局指标

主要结局

The study aims at bringing light on the Efficacy of the long standing traditional practice of Siddha Yogam Muraigal and Sadamanjil chooranam towards the management of Eraippu (Bronchial Asthma ).

时间窗: 48 DAYS

次要结局

  • The positive impact of Yoga in the management aspect may be highlighted through this study.(48 DAYS)

研究者

发起方
DR S SATHISH KUMAR
申办方类型
Other [self]

研究点 (1)

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