Prevalence and Molecular Identification of Human Schistosomiasis
1 other identifier
observational
359
0 countries
N/A
Brief Summary
Schistosomiasis remains one of the most important parasitic diseases of public health concern, particularly in developing countries including Egypt. It is caused by a trematode worm (blood flukes) of the genus Schistosoma
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2026
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 16, 2026
CompletedFirst Posted
Study publicly available on registry
March 19, 2026
CompletedStudy Start
First participant enrolled
May 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2027
March 19, 2026
March 1, 2026
1.3 years
March 16, 2026
March 16, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
prevalence of human schistosomiasis in the study participants
using conventional microscopic examination
24 hours
Study Arms (2)
Schistosoma haematobium
Urine filtration technique (10 ml urine) for diagnosis
Schistosoma mansoni
Direct wet mount and Kato-Katz thick smear technique (stool) for diagnosis
Interventions
DNA Sequencing and cox1 Gene Analysis of Schistosoma Isolates
Eligibility Criteria
All participants presented in Assiut Governorate hospitals
You may qualify if:
- Patients aged ≥ 5 years of both sexes attending Assiut Governorate hospitals during the study period.
- Patients clinically suspected of having schistosomiasis (urinary and/or intestinal) or referred for parasitological examination.
- Individuals (or guardians, in case of minors) who provide written informed consent.
- Patients willing to provide the required biological samples (urine and/or stool).
You may not qualify if:
- Patients Received praziquantel within the last 3 months before sample collection
- Patients with incomplete clinical or epidemiological data.
- Patients refusing participation or sample collection.
- Improperly collected, contaminated, or insufficient samples.
- Patients suffering from severe comorbid conditions that may interfere with the interpretation of results (e.g., advanced hepatic or renal failure).
- children with congenital urinary or intestinal anomalies.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principial investigator
Study Record Dates
First Submitted
March 16, 2026
First Posted
March 19, 2026
Study Start
May 1, 2026
Primary Completion (Estimated)
August 1, 2027
Study Completion (Estimated)
December 1, 2027
Last Updated
March 19, 2026
Record last verified: 2026-03