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NCT00463632 Clinical Trial

Schistosomiasis in Women of Reproductive Age in Burkina Faso: Implications for Control

Pregnancy Clinical Trial

Official title:
Schistosomiasis in Women of Reproductive Age in Burkina Faso: Implications for Control

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00463632
Other study ID # SRP-BF-ST-06
Secondary ID
Status Completed
Phase N/A
First received April 19, 2007
Last updated January 11, 2010
Start date January 2007
Est. completion date January 2009

Study information
Verified date January 2010
Source DBL -Institute for Health Research and Development
Contact n/a
Is FDA regulated No
Health authority Burkina Faso: Ministry of Health
Study type Observational

Clinical Trial Summary

Cross-sectional study of prevalence and intensity of schistosome infection in pregnant women, follow-up into postpartum, and the association of schistosome infection with haemoglobin concentration, compared to a group of non-pregnant women.

Description:

The objective of this study is to investigate the epidemiology of schistosomiasis and anaemia among pregnant and non-pregnant women in Burkina Faso and explore the implications for the national schistosomiasis control programme and future studies.

Specific objectives are:

- to determine the prevalence and intensity of schistosome infection in pregnant women attending for antenatal care and in non-pregnant women of reproductive age in an area which is hyperendemic for S.haematobium infection and in which there is little or no S.mansoni infection

- to determine the prevalence and intensity of schistosome infection in pregnant women attending for antenatal care and in non-pregnant women of reproductive age in an area in which S.mansoni infection is common

- to determine Haemoglobin concentration in pregnant women attending for antenatal care and in non-pregnant women of reproductive age in the regions described above

- to investigate the association between infection and haemoglobin concentration in pregnant and non-pregnant women

- to determine the prevalence of other parasitic infections in pregnant women and non-pregnant women including hookworms, ascaris, trichuris and malaria

- to demonstrate the research team's ability to follow-up pregnant women recruited at antenatal care clinics onto the postpartum period

Recruitment information / eligibility
Status Completed
Enrollment 200
Est. completion date January 2009
Est. primary completion date January 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 15 Years to 45 Years
Eligibility Inclusion Criteria:

- Pregnant women attending for ANC

- Non-pregnant women age 15-45 years accompanying relatives or children to the health centres or for immunization

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Burkina Faso Dori Health Centre Dori
Burkina Faso National Schistosomiasis Control Program Ouagadougou

Sponsors (2)
Lead Sponsor Collaborator
DBL -Institute for Health Research and Development Centre Muraz

Country where clinical trial is conducted

Burkina Faso, 

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