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AN OPEN CLINICAL TRIAL TO ASSESS THE EFFICACY OF SHUNTHI CHURNA IN THE MANAGEMENT OF AGNIMANDYA W.S.R. TO LOSS OF APPETITE IN CHILDREN

An open clinical trial to assess the efficacy of Shunthi churna in the management of Agnimandya w.s.r. to loss of appetite in children

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/12/010739
Enrollment
50
Registered
2017-12-04
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: null- Agnimandya(Loss of appetite)

Interventions

Intervention1: SHUNTHI CHURNA: SHUNTHI CHURNA IS AYURVEDIC DRUG MADE FROM ZINGIBER OFFICINALE, PART USED IS RHIZOME Drug dose - 1gm twice in a day Drug form - Churna Route of administration - Orally

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Children having age in between 14 to 16 years, irrespective to sex and religion. 2.Children presenting the features Agnimandya.

Exclusion criteria

Exclusion criteria: 1.Children having age less than 14 years and more than 16 years. 2.Patients suffering from any known acute or chronic illnesses that might interfere with study e.g acute infections, malignancies, thyroid problems etc. 3.Children having any associated life threatening medical or surgical disorders. 4.Children with any long term medications that may interfere with the result like for Diabetes etc will be excluded.

Design outcomes

Primary

MeasureTime frame
Shunthi churna will be effective in management of agnimandya in children.Timepoint: 15 days

Secondary

MeasureTime frame
To find a safe and effective drug in the management of Agnimandya (Loss of appetite) in childrenTimepoint: 15 DAYS

Countries

India

Contacts

Public ContactDrAshwinkumar Akshaylal Soni

K.L.E.U.â??s Shri B.M.K. Ayurveda Mahavidyalaya

azizarbar@gmail.com9844532113

Outcome results

None listed

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