Clinical trial Recruiting at 5 sites Observational Ages 6 to 90

Observing the epidemiology of visceral leishmaniasis in Emilia-Romagna

Official title: Visceral Leishmaniasis in Emilia-Romagna

Run by IRCCS Azienda Ospedaliero-Universitaria di Bologna · NCT06793111 · Data updated 2026-11-12

This study looks at the rise in cases of visceral leishmaniasis in Bologna to see how to improve diagnosis and treatment for patients of all ages.

Quick facts

Study typeObservational
Ages6 Years to 90 Years
SexAll
Enrollment300 (estimated)
SponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna
Academic / other
Locations5 sites (Cesena, Forlì-Cesena and 4 other locations)
StatusRecruiting
StartedApril 21, 2020
Main results expectedMay 31, 2025
Study endsDecember 31, 2025
Registry record updatedJanuary 27, 2025
Trial IDNCT06793111 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are patients of any age with a microbiologically confirmed diagnosis of visceral leishmaniasis.

Probably not a fit

Patients who do not provide informed consent will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to analyze the epidemiology of visceral leishmaniasis (LV) in the Province of Bologna, where there has been a noted increase in cases since 2012. By conducting a retrospective prospective analysis, the study seeks to establish a scientific basis for developing guidelines that standardize diagnostic and therapeutic approaches to LV. The goal is to reduce diagnostic delays and improve treatment outcomes, while also identifying new strategies for disease control to minimize transmission. The study will include patients of all ages with a confirmed diagnosis of LV who provide informed consent.

Why it matters

Potential benefit: If successful, this study could lead to improved diagnostic and treatment protocols for visceral leishmaniasis, ultimately enhancing patient outcomes.

How similar studies have gone: While there have been studies on leishmaniasis, this specific observational approach focusing on the epidemiology in a regional context is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients of any age with microbiologically established diagnosis of LV.
* Obtaining Informed Consent.

Exclusion Criteria:

* not having obtained Informed Consent

Where it's running

  • Ospedale M. Bufalini di Cesena, AUSL della Romagna
    Cesena, Forlì-Cesena, Italy
    Recruiting
  • Ospedale G.B. Morgagni L. Pierantoni di Forlì
    Forlì, Forlì-Cesena, Italy
    Recruiting
  • IRCCS Azienda Ospedaliero-Universitaria di Bologna
    Bologna, Italy
    Recruiting
  • Ospedale S. Maria delle Croci di Ravenna, AUSL della Romagna
    Ravenna, Italy
    Recruiting
  • Ospedale Infermi di Rimini, AUSL della Romagna
    Rimini, Italy
    Recruiting

Study contacts

  • Principal investigator: Pierluigi Viale, MD — IRCCS Azienda Ospedaliero-Universitaria di Bologna
  • Study coordinator: Pierluigi Viale, MD
  • Email: pierluigi.viale@unibo.it
  • Phone: +390512143353

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.