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Schistosomiasis in Women of Reproductive Age in Burkina Faso: Implications for Control
This study is currently recruiting participants.
Verified by DBL -Institute for Health Research and Development, April 2007
Sponsored by: DBL -Institute for Health Research and Development
Information provided by: DBL -Institute for Health Research and Development
ClinicalTrials.gov Identifier: NCT00463632
  Purpose

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.


Condition
Schistosomiasis
Anaemia
Pregnancy

MedlinePlus related topics: Anemia
U.S. FDA Resources
Study Type: Observational
Study Design: Screening, Cross-Sectional, Convenience Sample, Prospective Study
Official Title: Schistosomiasis in Women of Reproductive Age in Burkina Faso: Implications for Control

Further study details as provided by DBL -Institute for Health Research and Development:

Estimated Enrollment: 200
Study Start Date: January 2007
Detailed 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
  Eligibility

Ages Eligible for Study:   15 Years to 45 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

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
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00463632

Contacts
Contact: Seydou Touré, Dr (226) 50361017 schisto@liptinfor.bf

Locations
Burkina Faso
National Schistosomiasis Control Program Not yet recruiting
Ouagadougou, Burkina Faso, 06
Contact: Seydou Touré, Dr     (223)50361017     schisto@liptinfor.bf    
Principal Investigator: Hama Diallo, MD            
Dori Health Centre Recruiting
Dori, Burkina Faso
Sponsors and Collaborators
DBL -Institute for Health Research and Development
Investigators
Principal Investigator: Seydou Touré, MD The National Schistosomiasis Control Program Burkina Faso
  More Information

Study ID Numbers: SRP-BF-ST-06
Study First Received: April 19, 2007
Last Updated: April 19, 2007
ClinicalTrials.gov Identifier: NCT00463632  
Health Authority: Burkina Faso: Ministry of Health

Keywords provided by DBL -Institute for Health Research and Development:
schistosomiasis
anaemia
pregnancy

Study placed in the following topic categories:
Hematologic Diseases
Anemia
Schistosomiasis
Parasitic Diseases
Helminthiasis

Additional relevant MeSH terms:
Trematode Infections

ClinicalTrials.gov processed this record on January 16, 2009