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Effectiveness of kayyonyadi churna in the management of Pandu

Randomized controlled clinical trial to evaluate the efficacy of kayyonyadi churna in the management of pandu (iron deficiency anemia) - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/102983
Enrollment
80
Registered
2026-02-04
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

None listed

Sponsors

C.S.M.S.S Ayurved Mahavidhyalaya and Rugnalaya Aurangabad
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients having symptoms such as Daurbalya, Akshikutshotha, Panduta Pindikodweshtan, Hrutspandana. 2. Patient having Hb% more than 7 & less than 12gm/dl in females more than 8 & less than 13gm/dl in males. 3. Patients of age group between 18-45 years irrespective of gender, religion, socio-economic status, marital status, occupation. 4. Patient willing to give written informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnancy induced Anaemia. 2. Patients present with known case of Sickle cell Anemia, Megaloblastic Anemia, Aplastic Anemia, Pernicious Anemia. 3. Patients present with known case of any bleeding disorders, Thrombocytopenia, Hemorrhoids, Thalesemia. 4. Patient having systemic disorder like DM, HTN. 5. Patient having Hb below 7gm/dl irrespective of gender.

Design outcomes

Primary

MeasureTime frame
Daurbalya (General weakness) Panduta (Pallor) Hrutspandana (Palpitation) Lakshanas will be reducedTimepoint: 30 days

Secondary

MeasureTime frame
Akshikutshotha (Peri-orbital oedema) Pindikodweshtana(Leg cramps) Lakshanas will be reduced Timepoint: 30 days

Countries

India

Contacts

Public ContactDr Naresh Ramrao Nimbalkar

C.S.M.S.S Ayurved Mahavidhyalaya and Rugnalaya

ayushakti009@gmail.com9422711098

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026