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A comparative clinical study to evaluate the efficacy of Guda Nagaradi Gutika and Ferrous Sulphate in Pandu Vyadhi with special reference to Iron Deficiency Anaemia

A comparative clinical study to evaluate the efficacy of Gud Nagaradi Gutika and Ferrous Sulphate in Pandu Vyadhi with special reference to Iron Deficinecy Anaemia

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/048674
Enrollment
66
Registered
2023-01-02
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

Health Condition 1: D508- Other iron deficiency anemias

Interventions

None listed

Sponsors

Dr Javeriya Bashir Ahmed Naik
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Pandu vyadhi will be diagnosed on the basis of cardinal symptoms of pandu vyadhi (Panduta, dourbalya, agnimandya, akshikuta shotha, hritspandan) and hemogram. 2. Age: 18-60 years irrespective of gender, religion, socio-economic status, marital status 3. Haemoglobin: 8% or more than 8% and less than normal i.e. for males (less than 13g/dl), females (less than 12 g/dl) 4. MCV less than normal (80-100 fl)

Exclusion criteria

Exclusion criteria: 1. Known case of endocrine disorders like diabetes mellitus, hypothyroidism, Cushing syndrome, etc. 2. Pregnant and lactating ladies 3. Patient having tuberclusois, known case of HIV, leprosy, any type of cancer. 4. Patient showing signs and symptoms of internal bleeding, hemorrhoids,menorhagia etc

Design outcomes

Primary

MeasureTime frame
TO COMPARE THE EFFICACY OF GUD NAGARADI GUTIKATimepoint: 45 DAYS

Secondary

MeasureTime frame
TO OBSERVE THE ADVESE EFFECT OF GUD NAGARADI GUTIKA AND FERROUS SULPHATETimepoint: 45 DAYS

Countries

India

Contacts

Public ContactDr Javeriya Bashir Ahmed Naik

MAMs Sumatibhai Shah Ayurved Mahavidyalaya, Malwadi, Hadapsar, Pune

drsachinkumarpatil@yahoo.com9822603608

Outcome results

None listed

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