Study of Iron Absorption and Utilization in Asymptomatic Malaria
The Effect of Asymptomatic Malaria on Iron Absorption and Utilization From a Sorghum-based Meal in Adult Women in Benin
1 other identifier
interventional
23
1 country
1
Brief Summary
Anemia is still a main public health problem in sub-Saharan Africa. Anemic women have an increased maternal and perinatal mortality and anemic adults have diminished work capacity. In sub-Saharan Africa, the etiology of anemia is multifactoral; the major causes are low dietary bioavailability and chronic parasitic infections such as malaria. These causes are likely to interact because infection and infection-associated inflammation may impair the utilization and absorption of iron. Therefore, the control of parasite infections may be important to improve iron bioavailability from foods. Malaria infections are endemic in northern Benin. To investigate the contribution of asymptomatic malaria (a positive blood smear for malarial parasites but without clinical symptoms of fever, headache or malaise) to anemia, we are planning a human iron absorption study in Benin. We will recruit adults with asymptomatic malaria infection. The iron absorption and utilization of the study subjects will be studied while infected, then they will be treated to clear their infections, and then iron absorption and utilization will be restudied. Iron absorption will be determined by incorporation of labeled iron into erythrocytes, 14 days after the administration of a test meal containing labeled iron (stable isotope technique). Subjects will be men and non-pregnant, non-breastfeeding women with a body weight \< 65 kg and between the age of 18 - 30 years. The results of this study will provide important information on the influence of malaria infections on iron absorption and utilization in humans. The study will provide insight into the potential necessity of malaria control to ensure iron bioavailability from foods in developing countries.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for early_phase_1
Started Feb 2009
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2009
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2010
CompletedFirst Submitted
Initial submission to the registry
April 21, 2010
CompletedFirst Posted
Study publicly available on registry
April 22, 2010
CompletedJune 7, 2013
June 1, 2013
7 months
April 21, 2010
June 6, 2013
Conditions
Keywords
Study Arms (2)
Antimalarial treatment
EXPERIMENTALObservation
SHAM COMPARATORInterventions
Eligibility Criteria
You may qualify if:
- Age 18-35 y
- Body weight \< 65 kg
- A positive malaria smear (asexual P. falciparum parasitemia \> 500/μL blood) without clinical symptoms (fever or self-reported fever in last 7 days, headache, malaise)
- If female, not pregnant (tested by pregnancy test) and not breastfeeding
- No mineral and vitamin supplements two weeks before and during the study
You may not qualify if:
- Severe anemia (hemoglobin \< 8.0 g/dl)
- Chronic medical illnesses
- Blood donation or transfusion in the last 6 months before study time
- Soil-transmitted helminth infections (positive Kato-Katz-Smear)
- Tuberculosis (TB): The potential presence of TB will be excluded by a short health questionnaire (cough? night sweats? weight loss? close relative with TB?). If this questionnaire raises the possibility that the subject may be at risk for TB, he/she will be referred to the local medical service
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Swiss Federal Institute of Technologylead
- European Unioncollaborator
Study Sites (1)
Hopital de zone de Natitingou
Natitingou, Natitingou, 07, Benin
Related Publications (1)
Cercamondi CI, Egli IM, Ahouandjinou E, Dossa R, Zeder C, Salami L, Tjalsma H, Wiegerinck E, Tanno T, Hurrell RF, Hounhouigan J, Zimmermann MB. Afebrile Plasmodium falciparum parasitemia decreases absorption of fortification iron but does not affect systemic iron utilization: a double stable-isotope study in young Beninese women. Am J Clin Nutr. 2010 Dec;92(6):1385-92. doi: 10.3945/ajcn.2010.30051. Epub 2010 Oct 6.
PMID: 20926522DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Michael Zimmermann, Prof., MD
Human Nutrition Laboratory, Swiss Federal Institute of Technology
Study Design
- Study Type
- interventional
- Phase
- early phase 1
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Prof.
Study Record Dates
First Submitted
April 21, 2010
First Posted
April 22, 2010
Study Start
February 1, 2009
Primary Completion
September 1, 2009
Study Completion
April 1, 2010
Last Updated
June 7, 2013
Record last verified: 2013-06