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Development of nutraceutical ready to drink Navanga Yusha (ayurvedic soup)

Development of nutraceutical ready to drink Navanga Yusha and evaluation of its efficacy in alleviating Kaphaja Kasa – an exploratory study - NIL

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072094
Enrollment
20
Registered
2024-08-07
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: J22- Unspecified acute lower respiratory infection

Interventions

None listed

Sponsors

All India Institute Of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients between the age group of 20-40 years. Patients having kasa continuously not more then 15 days. Seasonal allergic cough included, Drug induced cough,Cough due to cold.

Exclusion criteria

Exclusion criteria: Patients of Kasa with any other pathology other than bronchitis. Patients with any other acute or chronic disease will be excluded from this study.(Broncial Asthma, Cough with fever, those on long term medications,Tuberculosis, cancer of bronchus, pleurisy, DM etc.). Pregnant and lactating mothers.

Design outcomes

Primary

MeasureTime frame
Development of Nutraceutical Ready to drink Navanga YushaTimepoint: 1 year

Secondary

MeasureTime frame
Reduction in clinical features of kaphaja kasa or Evaluation of Efficacy of Navanga Yusha in Alleviating Kaphaja Kasa Timepoint: 1.5 year

Countries

India

Contacts

Public ContactProf Dr Medha Kulkarni

All India Institute Of Ayurveda

Shivakumar.harti@aiia.gov.in9611275434

Outcome results

None listed

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