Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07482215

Prevalence and Molecular Identification of Human Schistosomiasis

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

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Sex eligibility

All sexes

Study type

Observational

About this study

Schistosomiasis has been diagnosed in Egypt since pharaonic times (3200 B.C.) by recovering Schistosome eggs and antigens in ancient mummies.In Egypt, Schistosoma mansoni and Schistosoma haematobium have historically been highly endemic, with widespread distribution along the Nile Delta and Valley.(4) Schistosoma haematobium is responsible for urogenital schistosomiasis, with hematuria as its primary manifestation, while Schistosoma mansoni, the prevalent species in Egypt, is causing intestinal schistosomiasis with liver-related sequelae

Who can participate

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

Inclusion criteria

  • 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).

Exclusion criteria

  • 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.

Treatment and study plan

Molecular phylogenetic and haplotype analysis

Diagnostic Test

DNA Sequencing and cox1 Gene Analysis of Schistosoma Isolates

Primary outcomes

  1. prevalence of human schistosomiasis in the study participants

    Time frame: 24 hours

    using conventional microscopic examination

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Official study title

Prevalence and Molecular Identification of Human Schistosomiasis With Assessment of Associated Epidemiological Risk Factors in Assiut Governorate, Egypt

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Mar 19, 2026
Registry last updated
Mar 19, 2026

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.

Published trials that share one or more normalized conditions with this study.