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Clinical Use of Drakshwaleha, an ayurvedic medicine in the treatment anemia due to iron deficiency.

Clinical Evaluation of Drakshavaleha in the Management of Pandu (Iron Deficiency Anaemia). - DIIDA

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/08/015146
Enrollment
60
Registered
2018-08-01
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: D508- Other iron deficiency anemias

Interventions

Intervention1: Drakshawleha: Dose : 10 gmtwice daily (with luke warm water) Dosage form : Awaleha Route of Administration : Oral Time of Administration : Morning and evening before meals Duration

Sponsors

Central Council For Research In Ayurvedic Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either sex aged between18 to 50 years. 2. IDA documented by hematologic indices. i. Hb 8gm-10gm. % ii. S.Ferritin iii. TIBC >450mcg/dL iv. S.Iron v. MCV vi. RDW >46fL vii. Reticulocyte count (Among these the first 3 are the essential criteria for inclusion) 3. Willing and able to participate for 112 days.

Exclusion criteria

Exclusion criteria: 1. Iron deficiency likely or definitely due to blood loss from the intestine or other sites. 2. History or evidence of intestinal malabsorption 3. Patients suffering from major systemic illness necessitating long term drug treatment (Rheumatoid arthritis, Psycho-Neuro-Endocrinal disorders, Bleeding disorders, etc.) 4. Other causes of Anemia (sickle cell disease, thalassemia, other hemolyticAnemia, bone marrow failure, etc.) apparent by history, physical examination, and/or laboratory tests. 5. Patients on prolonged ( > 6 weeks) medication with corticosteroids, antidepressants,anticholinergics, etc. or any other drugs that may have an influence on the outcome of the study. 6. Patients with concurrent serious hepatic disorder (defined as Aspartate AminoTransferase (AST) and / or Alanine Amino Transferase (ALT), Total Bilirubin, AlkalinePhosphatase (ALP) > 2 times upper normal limit), or Renal Disorders (defined as S. Creatinine >1.2mg/dL), Total Serum Cholesterol & / or Serum Triglycerides > 250 mg/dl, Severe PulmonaryDysfunction (uncontrolled Bronchial Asthma and / or Chronic Obstructive Pulmonary Disease[COPD]). 7. Alcoholics and/or drug abusers

Design outcomes

Primary

MeasureTime frame
Change in peripheral blood haemoglobin concentration.Timepoint: Time Frame: Every 4 weeks (on day 0, 28th,56th,84th and 112th)

Secondary

MeasureTime frame
Serum Ferritin level, Serum Iron level, TIBC level, MCV level, Reticulocyte count, Red blood cell Count, Any adverse events.Timepoint: Time Frame: Every 4 weeks (on day 0, 28th,56th,84th and 112th)

Countries

India

Contacts

Public ContactDr Vikas Nariyal

Regional Ayurveda Research Institute for Nutritional Disorders

vaidvikas.ayu@gmail.com9509560680

Outcome results

None listed

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