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Effectiveness of Siddha drug Aswaganthi Ilagam for the management of Veluppu noi (Iron deficiency Anemia) in children

An open non-randomized single arm, single centric clinical trial to evaluate the effectiveness of Siddha herbal formulation Aswaganthi ilagam for the management of Veluppu noi (Iron Deficiency Anemia) in children. - NA

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/055281
Enrollment
30
Registered
2023-07-17
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: D509- Iron deficiency anemia, unspecified

Interventions

Intervention1: Aswaganthi Ilagam: Dose: Age 5 -7 years : 260 mg BD Age 8 - 12 years:360 mg BD Duration : 48 days Control Intervention1: nil: nil

Sponsors

National Institute of Siddha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients willing to give blood specimen for lab investigations Haemoglobin level within 8.1 - 10.9 gm Blood smear shows microcytic hypochromic anemia Patients with signs such as Pallor of skin, mucous membrane, conjuctiva and nail beds and any two of following symptoms such as lack of concentration, malaise, anorexia, headache, palpitation

Exclusion criteria

Exclusion criteria: Patient with chronic disease Known case of any other hematological disorder Patient not willing to give blood sample for investigation

Design outcomes

Primary

MeasureTime frame
Primary outcome of the clinical study will be assessed by baseline increase in Hb level MCV MCH MCHC PCV & Serum Ferritin levels before & after treatmentTimepoint: 48th day

Secondary

MeasureTime frame
Physiochemical analysis of the drug will be standardisedTimepoint: 6 months

Countries

India

Contacts

Public ContactDr K Suresh

National Institute of Siddha

abiramipugaz@gmail.com9884657317

Outcome results

None listed

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