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Evaluation of Yavaksharadi Churna in adults with Tamaka Shwasa (Bronchial Asthma)

An Exploratory Clinical Study To Evaluate The Efficacy Of Yavaksharadi Churna In The Management of Tamaka Shwasa (Bronchial Asthma) In Adults - Nil

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106318
Enrollment
40
Registered
2026-03-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: J452- Mild intermittent asthma Health Condition 2: J453- Mild persistent asthma Health Condition 3: J454- Moderate persistent asthma

Interventions

None listed

Sponsors

Post Graduate Institute Of Ayurved Jodhpur Rajasthan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.The patients between the age group of 20 to 60 years of either sex presenting with clinical features of Tamaka Shwasa (Bronchial asthma) like, breathlessness, wheezing, paroxysm of attack, cough etc. irrespective of Sex and Religion. 2. Newly diagnosed cases of Bronchial Asthma having FEV1 and PEFR greater than 60 percent of predicted value. 3. Mild Intermittent, Mild Persistent and Moderate Persistent Cases of Bronchial Asthma (As per WHO GINA Guideline). 4. Patient willing to sign the consent form. 5. Never smokers.

Exclusion criteria

Exclusion criteria: 1. Age below 20 and above 60 years. 2. Patients having Acute exacerbation of Bronchial Asthma. 3. Patients having FEV1 and PEFR less than 60 percent of predicted value. 4. Diagnosed cases of Tuberculosis, Pneumonia, COPD and other acute and chronic pulmonary disorders. 5.Patients having asthma due to secondary causes such as drug induced like aspirin. 6. Pregnant women and lactating mothers. 7. Patients having concomitant systemic illness like Uncontrolled Hypertension, Poorly controlled Diabetes Mellitus, Renal failure, Malignancy, Acute or Chronic Liver Disease. 8. HIV positive cases.

Design outcomes

Primary

MeasureTime frame
Symptomatic ChangesTimepoint: 30th day and 45th day

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Bhagyashri Andhale

PGIA Dr Sarvepalli Radhakrishnan Rajasthan Ayurved University

bkmudgal9@gmail.com9460318138

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026