Health Condition 1: null- individuals with Iron Deficiency Anaemia (IDA)
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Subjects of both sexes in the age group of 18-70 years with Hemoglobin Subjects who have clinical symptoms such as pale skin colour, extreme fatigue, irritability, weakness, brittle nails, palpitation, headache, loss of appetite. Subjective improvement in quality of life in subjects with Iron deficiency anaemic. Subjects willing to give written informed consent. Subjects who have not participated in similar kind of study in last 3 months.
Exclusion criteria
Exclusion criteria: Subjects with hemoglobin concentration Blood hemoglobin level Absence of iron binding protein, hereditory spherocytosis and any association of severe complication. Pregnant & lactating women. Not willing to sign informed consent form.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in anaemia-related blood parameter levels An improvement in biochemical parameters viz. serum iron hemoglobin levels and erythrocyte counts. Improvement in symptoms such as skin pallor, tiredness and lack of energy, headache, weakness, low performance, appetite, breathlessness and feeling of wellbeing. Subjective improvement in quality of life in subjects with Iron deficiency anaemic. Timepoint: Patients will be followed up and the results were assessed from baseline on visit days: Visit 0- Baseline Visit 1 - At the end of Month 1 Visit 2- At the end of Month 2 (End of the study) | — |
Secondary
| Measure | Time frame |
|---|---|
| Compliance of the subject to the drug treatment and the adverse effects will be noted.Timepoint: Patients will be followed up and the results were assessed from baseline on visit days: Visit 0- Baseline Visit 1 - At the end of Month 1 Visit 2- At the end of Month 2 (End of the study) | — |
Countries
India
Contacts
Ramya Hospital