Clinical Study on mandurathi kudineer chooranam for the treatment of anaemia

Clinical Evaluation of Mandurathi kudineer chooranam for management of Azhal Veluppu Noi (iron deficiency anaemia)

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/05/019467

Enrollment

Registered

2019-05-31

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: D509- Iron deficiency anemia, unspecified

Interventions

Intervention1: Mandurathi Kudineer Chooranam: 30-60 ml twice a day after food for 90 days Control Intervention1: Nil: Nil

Eligibility

Inclusion criteria

Inclusion criteria: patients of confirmed diagnosis as an iron deficiency anaemia all anaemic patients approaching for siddha treatment at NIS OPD anaemic patients who are willing to take part in this study hemoglobin level ranges between 7 and 12 grams%

Exclusion criteria

Exclusion criteria: patients who are not confirmed as iron deficiency anaemia pregnancy and lactation persons having anaemia with other associated disorders such as renal failure, liver failure and ascites persons having known hypersensitivity to ingredients used in the study drug were excluded

Design outcomes

Primary

Measure	Time frame
improvement in the haemoglobin level, total RBC, PCV, MCV, MCH,MCHC,ESR and Smear studyTimepoint: improvement in the haemoglobin level, total RBC, PCV, MCV, MCH,MCHC,ESR and Smear study after 90 days	—

Secondary

Measure	Time frame
improvement in the clinical signs and symptomsTimepoint: 90 days	—

Countries

India

Contacts

Public ContactDr Sasi PriyaT

National institute of Siddha

svisu11@gmail.com9962542755

Outcome results

None listed

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