Actively Recruiting

Phase Not Applicable
Age: 15Years - 49Years
FEMALE
NCT07484256

MATCHING - feMAle geniTal sCHistosomiasis IN miGrants Female Genital Schistosomiasis in Migrants Presenting to an Outpatient Clinic in Italy: Prevalence and Clinical Impact

Led by IRCCS Sacro Cuore Don Calabria di Negrar · Updated on 2026-03-20

96

Participants Needed

1

Research Sites

127 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this study is to evaluate the prevalence of female genital schistosomiasis (FGS) in the migrant population with gynecological problems who access our center's dedicated outpatient clinic. Furthermore, we will address the relevance of FGS in women with clinical manifestations of the upper genital tract and evaluate the role of cervical-vaginal swabs in predicting upper genital tract involvement in schistosomiasis infection. The study is classified as experimental despite its descriptive objective of the prevalence of the infection of interest, as the vaginal swab and the PCR test performed on the swab and, if necessary, on the histological sample (collected during a possible interventional procedure performed for the patient's clinical needs) are not part of the standard clinical management of these cases but will be performed for the purposes of the study.

CONDITIONS

Official Title

MATCHING - feMAle geniTal sCHistosomiasis IN miGrants Female Genital Schistosomiasis in Migrants Presenting to an Outpatient Clinic in Italy: Prevalence and Clinical Impact

Who Can Participate

Age: 15Years - 49Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women aged 15 to 49 years
  • Origin from a country where Schistosoma infection is common
  • Having at least one symptom compatible with female genital schistosomiasis such as abnormal vaginal discharge, vaginal spotting or bleeding, genital itching or burning, pelvic pain or painful intercourse, genital ulcers, visible blood in urine, fertility problems, miscarriage or ectopic pregnancy, unexplained anemia, menstrual irregularities, or history of premature or low birth weight babies
  • Providing informed consent to participate and for personal data processing
Not Eligible

You will not qualify if you...

  • Refusal to give informed consent to participate in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

IRCCS Sacro Cuore Don Calabria hospital

Negrar, Verona, Italy, 37024

Actively Recruiting

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Research Team

E

Elvia Malo

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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