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A comparative study of Navayasa churna and Nisha Lauha in the treatment of Anaemia(Pandu)

A comparative study of Navayasa churna and Nisha Lauha in the management of Pandu w s r to Iron Deficiency anaemia

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/04/005695
Enrollment
60
Registered
2015-04-13
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: null- Iron Deficiency Anaemia

Interventions

Intervention1: Navayas churna: orally 2 Tab (1tab-250mg) twice a day after meal with Ghrit for 2 months follow up 1 month Control Intervention1: Nisha Lauha: orally 1 tab (250mg) twice a day aft

Sponsors

POST GRADUATE TEACHING HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1Patients between the age group of 15to50 years 2Patients having Cardinal symptoms of Pandu i e Panduta Pindikodvestana shrama Akshikutashoth Bhrama etc 3Patients having Hb% below the normal range In Men

Exclusion criteria

Exclusion criteria: 1Patients suffering from systemic disease like Diabetes Mellitus Renal disorders Heart disease cancer AIDS Hypertension etc and having bleeding disorders 2Patients having Anaemia due to chronic disease including inflammatory disease malignancy and chronic infection chronic blood loss 3Age less than 15 years and more than 50 years 4Hb level below 7g/dl 5pregnancy

Design outcomes

Primary

MeasureTime frame
Change in the clinical symptoms of Iron Deficiency Anaemia like Pallor sclera nail skin Periorbital oedema Anorexia Vertigo Weakness Dyspnoea on exertion Palpitation FatigueTimepoint: 2 MONTHS STUDY 1 MONTH FOLLOW UP

Secondary

MeasureTime frame
Change in Total Iron Binding Capacity S Iron S FerritinTimepoint: 2 MONTHS STUDY 1 MONTH FOLLOW UP

Countries

India

Contacts

Public ContactDr Hetal D Vyas

IPGT AND RA

vyashetal1979@gmail.com9427941558

Outcome results

None listed

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