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a study to evaluate the efficacy of different part of Shirisha plant in a semisolid dosage form (for e.g. like chyawanaprash) in the treatment of breathing problem (bronchial asthma)

Phase 2
Conditions
Health Condition 1: null- Tamaka Shwasa (Bronchial Asthama)
Registration Number
CTRI/2011/09/002010
Lead Sponsor
IPGT and RA
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
90
Inclusion Criteria

1.Both the sexes having age between 16 years to 60 years

2.Mild persistent cases of Asthma (as per WHO GINA Guideline) of duration more than 6 months.

3.Symptoms/exacerbation (Wheeze, cough and breathlessness) more than once a week but less than once a day in frequency.

4.Night symptoms twice a month but less than once a week.

Exclusion Criteria

Age more than 60 years and below 16 years

Patients having anaemia, pneumonia, tuberculosis, lung cancer, lung abscess and other such complicated conditions

Patients having diabetes, hypertension, Chronic and Acute renal failure etc. conditions in which urination is markedly diminished or excessive were excluded

HIV positive cases

Pregnant/lactating mother

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
PEFR <br/ ><br>Respiration Rate <br/ ><br>Breath Holding Time <br/ ><br>Differential count of Neutrophils <br/ ><br>Leukocytes <br/ ><br>Absolute eosinophil count(AEC) <br/ ><br>Timepoint: after 28 days
Secondary Outcome Measures
NameTimeMethod
exacerbation of signs and symptoms of Bronchial AsthmaTimepoint: 15 days
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