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Completed

NCT Number: NCT00463632

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

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.

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Key information

Age range

15 year–45 year

Sex eligibility

Female

Study type

Observational

Primary location

Dori Health Centre, Dori, Burkina Faso

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About this study

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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Sponsors and collaborators

Lead sponsor

DBL -Institute for Health Research and Development

Other

Collaborators

  • Centre Muraz

Registry information

Important dates

Study start
2007
Primary completion
2009
Study completion
2009
First posted
Apr 20, 2007
Registry last updated
Jan 12, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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