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Efficacy of indrashani choorna in pandu

Randomized controlled clinical trial of indrashani choorna in management of pandu roga with special reference of nutritional Deficiency Anemia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/06/034394
Enrollment
100
Registered
2021-06-25
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: - Health Condition 2: E639- Nutritional deficiency, unspecified

Interventions

Intervention1: Indrashani choorna in Pandu vyadhi: Indrashani choorna 960 mg with anupan Madhu for 30 days Control Intervention1: Kayyonyadi choorna in Pandu vyadhi: Kayyonyadi choorna 1.5gm with anup

Sponsors

Poonam sitaram Arjun
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age group between 16 to 60 years with irrespective to gender, religion, sex , socioeconomic conditions. 2. Patient of Pandu roga with rukshata,dourbalya,ayasen shwasa,hrutspandan,akshikuta shoth 3. HB % - Female - Male - <7 gm/dl to 12 gm/dl

Exclusion criteria

Exclusion criteria: Age group below 16 and above 60 years. 2. Patients other than Nutrition deficiency Anemia. 3. Anemia due to other pathology like cardiac, renal , diabetes mellitus, acute and chronic blood loss. 4. Pregnant woman and lactating woman.

Design outcomes

Primary

MeasureTime frame
To determine the efficacy of indrashani choorna in Pandu vyadhiTimepoint: 4 weeks—

Secondary

MeasureTime frame
To review the literature of Pandu vyadhiTimepoint: 4 weeks—

Countries

India

Contacts

Public ContactPoonam sitaram Arjun

Hon. Shree annasaheb dange ayurveda medical collegeand post graduation research center , ashta

drdattatraynikam@gmail.com8390761674

Outcome results

None listed

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