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 type | Observational |
|---|---|
| Ages | 6 Years to 90 Years |
| Sex | All |
| Enrollment | 300 (estimated) |
| Sponsor | IRCCS Azienda Ospedaliero-Universitaria di Bologna Academic / other |
| Locations | 5 sites (Cesena, Forlì-Cesena and 4 other locations) |
| Status | Recruiting |
| Started | April 21, 2020 |
| Main results expected | May 31, 2025 |
| Study ends | December 31, 2025 |
| Registry record updated | January 27, 2025 |
| Trial ID | NCT06793111 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
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Immunogenicity screening of Leishmania vaccine candidate antigens in Ethiopian patients
This study tests whether six Leishmania vaccine candidate antigens can trigger T-cell responses in patients with cutaneous or visceral leishmaniasis.
-
Pediatric leishmaniasis in Italy: clinical and treatment patterns
This project will collect medical information to see how leishmaniasis presents and is treated in children under 18 in Italy.
-
Risk factors for outcomes after surgery for very large intrathoracic tumors
This study tests how patients with very large chest tumors fare after surgical removal, to see which factors are linked to better or worse outcomes.
-
IBS and rosacea in adults: how common is rosacea among people with IBS at a university center
This observational study tests how often rosacea occurs in adults with IBS who are treated at a university hospital in Bologna.
-
INSL3 as a Biomarker to See If Puberty Has Started
Researchers are testing whether a single blood test for INSL3 can tell if a child’s puberty has begun, potentially reducing need for the GnRH stimulation test.
-
Ultrasound-guided pelvic floor training to help birth in first-time pregnant women
This study tests if real-time ultrasound feedback on pelvic floor muscles during labor preparation helps shorten the second stage of labor in first-time pregnant women with specific pelvic floor muscle activation.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.