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Effect of Ferrous Sulphate in improving the haemoglobin levels of blood donors in Southern Senatorial District of Cross River Sate, Nigeria.

Effect of Ferrous Sulphate in improving the haemoglobin levels of blood donors in Southern Senatorial District of Cross River Sate, Nigeria.

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
PACTR
Registry ID
PACTR202412542319813
Enrollment
140
Registered
2024-12-09
Start date
2024-09-02
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Haematological Disorders

Interventions

Ferrous sulphate and vitamin C supplements.
Ferrous Sulphate

Sponsors

Egeonu Yochi Immaculata
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Absence of signs of fatigue, weakness, normal skin colour and mucous membranes with no jaundice, cyanosis. Absence of clinical signs of disease/ill health (HIV, malaria, sickle cell). Having a weight more than 50 kg. Male and female blood donors within the age bracket of 18 to 59 years. Female having no menstrual cycle. Willingness to give informed consent to the study. Blood donors who are resident in Calabar metropolis irrespective of place of birth, educational, religious and ethnic, background. Blood donors who are present at the designated health facilities. Blood donors aged (18-59) years, who are not already taking iron and vitamin C tablets.

Exclusion criteria

Exclusion criteria: All blood donors aged below 18 and above 59 years, who do not meet the inclusion criteria pregnant and lactating women female blood donors on menstrual cycles having a weight less than 50 kg, mentally vulnerable Donors with conditions associated with gastrointestinal blood loss a personal or family history of hereditary hemochromatosis, cancer.

Design outcomes

Primary

MeasureTime frame
i.At least 90% improvement in mean levels of haemoglobin, PCV, and meam cell haemoglobin concentration of the study subjects. ii. At least 85% of the study subjects should understand anaemia and its symptoms.Iii. At least 85% of the study subjects should know about the preventive measures of anaemia.

Secondary

MeasureTime frame
i. Subjects must demonstrate at least 80% adherence to supplements with assessment of compliance and self-reported side effects. ii.At least 90% of the subjects will resolve to take up and adhere to anaemia treatment option after blood donation.

Countries

Nigeria

Contacts

Public ContactMagaret Akpan

Senior Lecturer

Magginem2000@yahoo.com+2347068534593

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026