A clinical trial to study the effect of two drugs in Anemic females between reproductive age group.

Effect of Majun e khabsul hadeed in iron deficiency anemia in women of reproductive age group- A randomised standard controlled study

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/03/012759

Enrollment

Registered

2018-03-22

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- Aneamia in reproductive age group Health Condition 2: D509- Iron deficiency anemia, unspecified Health Condition 3: D509- Iron deficiency anemia, unspecified Health Condition 4: D509- Iron deficiency anemia, unspecified Health Condition 5: D509- Iron deficiency anemia, unspecified Health Condition 6: D509- Iron deficiency anemia, unspecified

Interventions

Intervention1: Majun Khabsul hadeed: 5gm once in a day orally for 3 months Control Intervention1: Cap. Fefol: 1 cap Once daily orally for 3 months

Eligibility

Inclusion criteria

Inclusion criteria: Patients with Age group 18-45 and Hemoglobin in the range of 8-11.9 gm%

Exclusion criteria

Exclusion criteria: Patients with Hemoglobin less than 8gm%, H/o acute blood loss, Systemic diseases,Pregnant and lactating women.

Design outcomes

Primary

Measure	Time frame
Change in subjective parametersTimepoint: 3 months	—

Secondary

Measure	Time frame
Change in objective parametersTimepoint: 3 months	—

Countries

India

Contacts

Public ContactIram Bushra

Rajiv gandhi university of health science

kouser2fathima@gmail.com9743730208

Outcome results

None listed

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