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Role of PRIYALADI GRANULES and HYDERABAD MIX in undernutrition in children.

A Randomised comparative clinical trial to evaluate the efficacy of Priyaladi Granules and Hyderabad Mix in karshya (Undernutrition) in children. - NIL

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100719
Enrollment
40
Registered
2026-01-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: E441- Mild protein-calorie malnutrition

Interventions

None listed

Sponsors

State Ayurvedic College and Hospital Lucknow
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Individuals of both genders male and female children between age group of 3 to 12 years. Individual fulfilling the description of Karshya described in our texts like Shushka Sphika,Shushka Udara, Shushka Griva, Dhamani Jal Darshan. Parents of patient willing to participate in the trial. Religious Background, All religions included. Socioeconomic Status, All strata considered. Nutritional Status, Only children classified poor weight gain, lean and thin body as per having mild to moderate malnutrition based on Indian Academy of Pediatrics IAP grading were included

Exclusion criteria

Exclusion criteria: Children diagnosed or suspected to have infectious diseases such as tuberculosis. Children with congenital anomalies or hereditary disorders. Children with malignancies or known immunodeficiency syndromes. Children weighing less than 60 percent of the ideal weight for age. Children classified as severely or very severely malnourished. Children with known cardiac, renal, hepatic, or endocrine disorders. Children with any systemic illness that could interfere with the proposed treatment. Less than 3 and more than 12 year s of age.

Design outcomes

Primary

MeasureTime frame
To determine the role Trial drug in the management of Karshya in children in four months.Timepoint: In 90 day of trial.

Secondary

MeasureTime frame
Assessment of anthropometric parameter in enrolled patient of karshya Assess the comparative effect between both drugs.Timepoint: In 120 day of trial.

Countries

India

Contacts

Public ContactDr Deepak Kumar

State Ayurvedic college and hospital Lucknow

deepakwhynot@gmail.com09509074322

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026