A clinical trial to evaluate the efficacy of Vajra Vatak Mandoor and Tapyadi Loha Vati in the management of Iron deficiency Anaemia

A randomized comparative clinical trial to evaluate the efficacy of Vajra Vatak Mandoor and Tapyadi Loha Vati in the management of Pandu with special reference to Iron deficiency?anaemia - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/08/093137

Enrollment

Registered

2025-08-18

Start date

Unknown

Completion date

Unknown

Last updated

2025-09-15

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

Eligibility

Inclusion criteria

Inclusion criteria: 1. Biochemical Parameters - Hb%:- Female: 7-10% gm/dl Male: 7-11% gm/dl 2. Patients having 3 or more symptoms such as Panduta (Pallor),Akshikoot shoth (Periorbital Oedema), Aayasen Shwas (Dyspnoea on exertion),Dourbalya (Weakness) , Bhrama (Giddiness)

Exclusion criteria

Exclusion criteria: CRITERIA FOR EXCLUSION 1. Known cases of cirrhosis of the liver, ascites, alcoholic liver disease in adults, and children 2. Pregnant and lactating mother. 3. Known case of Uncontrolled Diabetes mellitus 4. Chronic Kidney Disease 5. Known cases of - HIV, Aplastic Anaemia, Pernicious Anaemia, megaloblastic anaemia, Sickle cell anaemia and thallasemia, Sideroblastic Anaemia, leukaemia, Metastasis cancer. 6. Patient receiving care from another physician for the same issue.

Design outcomes

Primary

Measure	Time frame
To compare the efficacy of Vajra vatak mandoor and Tapyadi loha vati on Objective increasing Hb% given for 60 days in the management of Pandu w.s.r to Iron deficiency anaemia. Timepoint: at day 15,30,45,60 days	—

Secondary

Measure	Time frame
1.To compare the efficacy of Vajra vatak mandoor and Tapyadi loha vati for reducing symptoms given for 60 days in the management of Pandu w.s.r to Iron deficiency anaemia. 2. To observe and compare the adverse effects in two groups within 60 days.Timepoint: at day 15,30,45,60 days	—

Countries

India

Contacts

Public ContactDr Vrinda Kurande

PDEAs College Of Ayurved And Research Centre Kayachikitsa Department Third Floor Nigdi Pune

vrinda.kurande@gmail.com7722030521

Outcome results