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Effect of Ayurvedic drugs on iron deficiency Anaemia during Pregnancy

A CLINICAL STUDY ON GARBHINI PANDU (WITH SPECIAL REFERENCE TO IRON DEFICIENCY ANEMIA IN PREGNANCY) & ITS MANAGEMENT WITH PUNARNAVA MANDURA & DHATRI LAUHA

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/07/006049
Enrollment
35
Registered
2015-07-27
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: null- Garbhini Pandu-Iron Deficiency Anaemia during Pregnancy

Interventions

Intervention1: Punarnava Mandura: 2 tablets(500mg each) t.d.s., before meal with Takra (Butter Milk) for 90 days Control Intervention1: Dhatri Lauha: 2 tablets(500mg each) t.d.s., before meal with Lu

Sponsors

Institute of Postgraduate Teaching and Research in Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.The pregnant woman age group from 19 to 40 years having clinical signs & symptoms of Garbhini Pandu i.e., Panduta, Bhrama, Daurbalya, Shwasa, etc. described in Ayurvedic classics & modern literature. 2.Patients of 2nd or 3rd trimester of pregnancy 3. Patients having Hemoglobin (Hb% )equal to or less than 10gm% in 2nd and less than 11gm% in 3rd trimester and more than 6.5gm%

Exclusion criteria

Exclusion criteria: 1.Patients suffering from pregnancy related complications like PIH, hyper emesis gravidarum, pre eclampsia etc. 2.1st trimester of pregnancy. 3.Patients having with high risk pregnancy. 4.Patients having Hb% count less than 6.5gm% & more than 10gm%.

Design outcomes

Primary

MeasureTime frame
â?¢Improvement in signs and symptoms of Garbhini Pandu. â?¢Increase in Hb% Timepoint: 90 days

Secondary

MeasureTime frame
Improvement in other biological parametersTimepoint: 90 days

Countries

India

Contacts

Public ContactDr Shilpa B DONGA

Institute for postgraduate teaching and research in ayurveda

deepika.yati@gmail.com7405674312

Outcome results

None listed

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