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A Clinical Trial Comparing Homoeopathy and Standard Iron Therapy In Young Adults With Anemia.

A Randomized Controlled Trial On The Efficacy Of Homoeopathic Treatment In Comparison To Standard Iron Preperation For Iron Deficiency Anemia In Young Adults - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093302
Enrollment
60
Registered
2025-08-20
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: D508- Other iron deficiency anemias

Interventions

Intervention1: INDIVIDUALIZED HOMOEOPATHIC MEDICINES: Participants will receive 1 grain weight of Saccharum lactis impregnated with 2 drops of individualized Homoeopathic medicine, administered once w

Sponsors

White Memorial Homoeo Medical College And Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Young adults aged 20-24 years. Confirmed iron deficiency anemia based on hematological markers (Hemoglobin less than 12 g per dL, serum ferritin less than 15 ng per mL). Residency in the study region (e.g., Kanniyakumari, Tamil Nadu). Those who are eligible for the trial.

Exclusion criteria

Exclusion criteria: Individuals with hemoglobin levels below 7 g per dL who require urgent intervention, such as Intra venous iron or transfusion. Individuals who have chronic diseases affecting iron metabolism, iron absorption, iron overload disorders. Individuals who are taking iron supplements or Homoeopathic remedies for anemia within the past 6 months. Pregnant or Lactating women. Female Participants who have irregular menstrual cycles with menorrhagia or pathologic blood loss (to reduce confounding from chronic loss). Recent major surgery or trauma within the past three months. Use of medications interfering with iron absorption, such as proton pump inhibitors (PPIs) or chronic corticosteroid use. Substance abuse or chronic alcoholism.

Design outcomes

Primary

MeasureTime frame
Change in serum ferritin level, Symptom resolutionTimepoint: Serum Ferritin - Baseline (Month 0), Month 3 (Week 12), Month 6 (Week 24). Symptom resolution- Monthly intervals: Month 1 (Week 4), Month 2 (Week 8), Month 3 (Week 12), Month 4 (Week 16), Month 5 (Week 20), Month 6 (Week 24).

Secondary

MeasureTime frame
Identification of effective Homoeopathic remedies. Treatment adherence. Patient satisfaction. Incidence of side effects. Relapse rateTimepoint: Identification of effective Homoeopathic remedies-Continuous throughout treatment; Final evaluation at Month 6 (Week 24). Treatment adherence - Monthly reviews: Month 1?6 (Weeks 4, 8, 12, 16, 20, 24); Final review at Month 6 (Week 24). Patient satisfaction -Month 3 (Week 12), Month 6 (Week 24). Incidence of side effects-Continuous monitoring; Monthly reviews: Month 1?6 (Weeks 4, 8, 12, 16, 20, 24). Relapse rate-Month 9 (Week 36) ? 3 months post-intervention.

Countries

India

Contacts

Public ContactDr PRIYA RAJINI R M

White Memorial Homoeo Medical College and Hospital

drpriyarm@gmail.com7598188281

Outcome results

None listed

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