The effects of iron complementary on hemoglobin level and mood

Not Applicable

• Conditions: Anemia.; Iron deficiency anaemia

• Registration Number: IRCT201210137618N4
• Lead Sponsor: Deputy of Research, Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 225

Inclusion Criteria

Students living in dormitories of Tabriz university of medical sciences, Not using vitamin and iron complementary in the last 3 month, Not using oral or injection steroidal hormones, Not using IUD, Not existence of a hepatic, infectious or parasitic diseases in the time of study, Not existence of hematologic disorders such as thalassemia or hemophilia, any contraindication iron complementary, Not existence psychological disorders, Not existence systemic disorders which can affect menstrual bleeding such as diabetes, thyroid disorders, hyperadrenalism,… , participants with signs and symptoms of anemia which investigator finds in clinical examination( assessing color of mucosa, nails, conjunctive), participants with hemoglobin below 12g/dl.
Exclusion criteria: Not being interested to continue (leaving study), diagnosis of other types of anemia during the study, diagnosis of systemic, infectious, parasitic or hepatic disorders during study.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Hemoglobin level. Timepoint: Once before the intervention and second time 4 months after beginning the intervention. Method of measurement: Based on result laboratory by Cell counter device model H1.;Mood. Timepoint: Once before the intervention and second time 4 months after beginning the intervention. Method of measurement: Based on POMS SF questionnaire.

Secondary Outcome Measures

Name	Time	Method
Menstrual bleeding level. Timepoint: Once before the intervention and second time 4 months after beginning the intervention. Method of measurement: Based on Higham questionnaire.