NCT01108939

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
23

participants targeted

Target at P25-P50 for early_phase_1

Timeline
Completed

Started Feb 2009

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2009

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2009

Completed
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2010

Completed
20 days until next milestone

First Submitted

Initial submission to the registry

April 21, 2010

Completed
1 day until next milestone

First Posted

Study publicly available on registry

April 22, 2010

Completed
Last Updated

June 7, 2013

Status Verified

June 1, 2013

Enrollment Period

7 months

First QC Date

April 21, 2010

Last Update Submit

June 6, 2013

Conditions

Keywords

Malaria, Iron absorption, Iron utilization, Benin

Study Arms (2)

Antimalarial treatment

EXPERIMENTAL
Drug: Antimalarial treatment

Observation

SHAM COMPARATOR
Other: Observation

Interventions

Antimalarial treatment
Observation

Eligibility Criteria

Age16 Years - 35 Years
Sexfemale
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

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

Study Sites (1)

Hopital de zone de Natitingou

Natitingou, Natitingou, 07, Benin

Location

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.

MeSH Terms

Conditions

Malaria, FalciparumMalaria

Interventions

Observation

Condition Hierarchy (Ancestors)

Protozoan InfectionsParasitic DiseasesInfectionsMosquito-Borne DiseasesVector Borne Diseases

Intervention Hierarchy (Ancestors)

MethodsInvestigative Techniques

Study Officials

  • Michael Zimmermann, Prof., MD

    Human Nutrition Laboratory, Swiss Federal Institute of Technology

    PRINCIPAL INVESTIGATOR

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

Locations