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Study to see the effect of oral intake of Kantakari Kwath in the treatment of Cough

Single Arm Study To Evaluate The Effect Of Kantakari Kwath In Kasa

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/11/029111
Enrollment
45
Registered
2020-11-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: J398- Other specified diseases of upperrespiratory tract

Interventions

Intervention1: Kantakari Kwath 40 ml Twice a day for 9 days ,after food.: Kantakari churna 20 gm will be boiled in 320 ml water and it will be reduced to 40ml.After filtration,1 gram of Pippali churna

Sponsors

Rashmi Kurbet
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients suffering from Kasa(more than 7 days),irrespective of season and prakriti .

Exclusion criteria

Exclusion criteria: 1.Patients with fever or any other COVID symptoms 2.Patients having cough with blood and with complication of Kasa i.e Chronic obstructive Bronchitis,Lung Cancer,Tuberculosis,Bronchiectasis,Lung abscess,Pulmonary edema resulting from Cardiac and Renal disease,Pneumonia will be excluded. 3.Patients with severe form of other systemic disorders like Cardiac disease,Renal failure,CVA,immuno-compromised diseases etc.will be excluded. 4.Pregnant women and lactating mothers. 5.Surgical indication. 6.Kshataj and Kshayaj kasa.

Design outcomes

Primary

MeasureTime frame
Kantakari kwath is effective in management of Kasa.(Objective parameters-CBC,ESR, CXR & Subjective parameters based on symptoms)Timepoint: Oral intake of 40 ml Kantakari Kwath,twice a day for 9 days, with 3 follow ups(0,3,6,9)

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactRashmi Kurbet

Dr D Y Patil College Of Ayurveda And Research Centre,Pimpri,Pune

vjayu82@gmail.com8983478062

Outcome results

None listed

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