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Schistosoma Haematobium Infections and Praziquantel

Schistosoma Haematobium Infections Among Schoolchildren in Central Sudan One Year After Treatment With Praziquantel

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01558336
Enrollment
520
Registered
2012-03-20
Start date
2008-08-31
Completion date
2012-09-30
Last updated
2013-01-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Schistosomiasis

Keywords

Schistosoma haematobium, schoolchildren, Central Sudan, Praziquantel

Brief summary

The purpose of this study is to evaluate the impact of praziquantel for the treatment of Schistosoma haematobium infection among schoolchildren in Al Salamania in Central Sudan.

Detailed description

A longitudinal study will be conducted to evaluate the impact of praziquantel for the treatment of Schistosoma haematobium infection among schoolchildren in Al Salamania in Central Sudan. A cohort of schoolchildren (6-15 years of age) was investigated before and 1 year after treatment with a single dose of praziquantel 40mg/kg.

Interventions

DRUGpraziquantel

praziquantel 40 mg/kg oral tablets

Sponsors

Hikma Pharmaceuticals LLC
CollaboratorINDUSTRY
University of Khartoum
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Years to 15 Years
Healthy volunteers
No

Inclusion criteria

* School children

Exclusion criteria

* Taking praziquantel

Design outcomes

Primary

MeasureTime frameDescription
cure rateone yearThe reduction of the prevalence and intensity of S.haematobium infection following a single dose of praziquantel40mg/kg

Secondary

MeasureTime frameDescription
reduction in the intensity of infection byone yearwill a single dose of PZQ significantly reduced intensity of infection of S. haematobium infection 1 year after treatment

Countries

Sudan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026