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Clinical Trials/CTRI/2019/06/019745
CTRI/2019/06/019745
Not yet recruiting
Phase 2

A Comparative Study to Evaluate the Efficacy of Shwasahara Mahakashaya Avleha w.r.to Shwasahara Mahakashaya choorna in Tamaka Shwasa w.s.r to Childhood Bronchial Asthmaâ??An open ended, double armed, Randomized, Controlled Clinical Trial.

All India Institute of Ayurveda0 sites0 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Health Condition 1: J454- Moderate persistent asthma
Sponsor
All India Institute of Ayurveda
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\)Individuals of either gender between age group of 5 to 15 years.
  • 2\)Diagnosed cases of Tamaka Shwasa â??bronchial asthma with at least 3 episodes of asthma symptoms (cough, breathlessness) during the previous year.
  • 3\)Severity as mild to moderate stable bronchial asthma (Tamaka Shwasa) as per W.H.O GINA Guidelines.
  • 4\)Patient on other drug therapy will be included only after completion of the washout period of 3 weeks.
  • 5\)Parents giving consent to participate in study.

Exclusion Criteria

  • 1\.Individuals below 5 years and above 15 years of age.
  • 2\.Sever case like status asthmaticus.
  • 3\.Evidence of active concomitants pulmonary disease other than asthma.
  • 4\.Evidence of requirement of intubation for asthma, or had been hospitalized for asthma within 1 month before. Had unresolved sinus disease or an unresolved upper or lower respiratory tract infection within 3 weeks. 5\.More than 4 short courses of oral corticosteroids within the year preceding the screening visit or any oral corticosteroids in the preceding 4 weeks.
  • 6\.Concomitant severe decompensated systemic disease (cardiovascular, renal, hepatic, endocrine, haematological, neurological, immunological).
  • 7\.Patient/Parents not willing to participate in the study.

Outcomes

Primary Outcomes

Not specified

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