Assessment of Anaemia Attributable to Schistosomiasis in School Children in Kenya: Mechanisms and Effect of Treatment
NCT ID: NCT00414479
Last Updated: 2010-01-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
1500 participants
OBSERVATIONAL
2006-07-31
2010-01-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Iron Supplementation in Schistosomiasis and Soil Transmitted Helminths Control Programmes in Zambia
NCT00276224
Schistosome and Intestinal Worm Infections and Malaria Morbidity Among School and Pre-school Children in, Tanzania
NCT00347113
Iron Absorption and Utilization in Adolescents Infected With Malaria Parasites, Hookworms or Schistosoma
NCT01163877
Health Benefits of Repeated Treatment in Pediatric Schistosomiasis
NCT01424410
Schistosoma Haematobium Infections and Praziquantel
NCT01558336
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
children 9-12 years of age
Children with schistosomiasis, malaria and anaemia
praziquantl, iron, ACT
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
praziquantl, iron, ACT
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
9 Years
12 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
DBL -Institute for Health Research and Development
OTHER
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Diana Karanja, DR
Role: PRINCIPAL_INVESTIGATOR
Kenya Medical Research Institute
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Kenya Medical Research Institute
Kisumu, , Kenya
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
SRP-KY-DK-06
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.