STUDY TO EVALUATE THE EFFICACY OF MURVADYA CHURNA IN PANDU

?RANDOMISED OPEN CONTROLLED CLINICAL TRIAL TO EVALUATE THE EFFICACY OF MURVADYA CHURNA IN PANDU - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/09/073355

Enrollment

100

Registered

2024-09-04

Start date

Unknown

Completion date

Unknown

Last updated

2024-09-16

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: Patient with sign and symptoms of Panduta,Daurbalya,Shwas,Bhrama (Shram Bhramni-pidita),Aruchi (Anorexia), Gauravam (Heaviness of the body),Pindikodveshtan, Shunakshikuta

Exclusion criteria

Exclusion criteria: Pregnant women, Lactating mothers. Anaemia associated with other known history of diseases like Liver Cirrhosis, Ascites, Congestive Cardiac Failure, Acute Coronary Syndromes, AIDS, Tuberculosis, Malignancy, Helminthic infection , known history of Chronic Blood loss conditions

Design outcomes

Primary

Measure	Time frame
To study the effect of Murvadya Churna in Pandu vyadhiTimepoint: 90days	—

Secondary

Measure	Time frame
The improvement in the patients will be assessed on the basis of relief in signs and symptoms of Pandu. For this assessment the main signs and symptoms will be given in gradation depending upon their severity and all the parameters of assessment before and after the follow up day will be taken into consideration to assess the effectiveness of the treatment . To study etiopathology of Pandu in detail according to ayurveda To improve quality of life & reduce discomfort of patient To achieve the outcome of study in 90 daysTimepoint: 90days	—

Measure

Time frame

The improvement in the patients will be assessed on the basis of relief in signs and symptoms of Pandu. For this assessment the main signs and symptoms will be given in gradation depending upon their severity and all the parameters of assessment before and after the follow up day will be taken into consideration to assess the effectiveness of the treatment . To study etiopathology of Pandu in detail according to ayurveda To improve quality of life & reduce discomfort of patient To achieve the outcome of study in 90 daysTimepoint: 90days

—

Countries

India

Contacts

Public ContactDr Pradnya Bhaskar Mali

Yashwant Ayurvedic college post graduate training and research center kodoli

drdipaliswamis@gmail.com9960003947

Outcome results