AzTrials
AzTrials

SchistosomiasisNCT07482215

Prevalence and Molecular Identification of Human Schistosomiasis

An observational study of Schistosomiasis, run by Assiut University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Official record

Search all trials

Trial 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 Read more about this study

Who is it for?
Any age
Conditions the study is for
Schistosomiasis
What is being tested?
Molecular phylogenetic and haplotype analysis
How many people
359 participants
Where
No sites listed yet
Study dates
May 2026to Dec 2027
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Child, Adult, Older adult

Study population: All participants presented in Assiut Governorate hospitals

Who may be able to join

  • 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).

Who cannot join

  • 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.

About this study

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

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

Read the detailed description

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

Conditions
Schistosomiasis
Being tested
Molecular phylogenetic and haplotype analysis
Medical subject headings
Schistosomiasis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Molecular phylogenetic and haplotype analysisDiagnostic test

    DNA Sequencing and cox1 Gene Analysis of Schistosoma Isolates

Study groups in NCT07482215
Study groupRoleWhat they receive
Schistosoma haematobiumUrine filtration technique (10 ml urine) for diagnosis
Receives: Diagnostic Test: Molecular phylogenetic and haplotype analysis
Schistosoma mansoniDirect wet mount and Kato-Katz thick smear technique (stool) for diagnosis
Receives: Diagnostic Test: Molecular phylogenetic and haplotype analysis

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. prevalence of human schistosomiasis in the study participants

    using conventional microscopic examination

    Measured: 24 hours

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Mar 2026
  2. Study startMay 2026 (estimated)
  3. Primary completionAug 2027 (estimated)
  4. Study completionDec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
359 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07482215
Sponsor's protocol ID
PMHS
Status last verified
Mar 2026
First submitted
16 Mar 2026
Last updated
19 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in