Biobank for patients with infectious and tropical diseases
Creation of a Bank of Biological Materials and Associated Data Related to Patients With Infectious and Tropical Diseases
IRCCS Sacro Cuore Don Calabria di Negrar · NCT05770765
This study is setting up a biobank to collect and store samples from patients with infectious and tropical diseases, as well as healthy volunteers, to help with future research and treatments.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 60000 (estimated) |
| Sex | All |
| Sponsor | IRCCS Sacro Cuore Don Calabria di Negrar (other) |
| Locations | 1 site (Negrar, Verona) |
| Trial ID | NCT05770765 on ClinicalTrials.gov |
What this trial studies
This project establishes the TROPICA-BIOBANK, which collects and stores biological samples and associated data from patients suspected of having infectious or tropical diseases, as well as healthy volunteers. Samples include various human biological matrices, DNA, protein extracts, and other materials, all stored securely at -80°C for up to 40 years. The biobank aims to support future research and clinical trials by providing a rich resource of biological materials. Quality control measures are in place to ensure the integrity of the samples over time.
Who should consider this trial
Good fit: Ideal candidates include patients visiting the Department of Infectious and Tropical Diseases with suspected infections, as well as healthy volunteers over the age of 18.
Not a fit: Patients with a history of alcohol or drug abuse, or those who are pregnant or breastfeeding, may not benefit from this study.
Why it matters
Potential benefit: If successful, this biobank could enhance research and treatment options for infectious and tropical diseases by providing valuable biological materials for analysis.
How similar studies have performed: While biobanks for infectious diseases are common, the specific approach and focus of this biobank may offer novel insights and resources for future research.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: • Informed consent (for healthy volounteers also: age \> 18 years, health status ascertained by laboratory tests, electrocardiogram and medical examination) Exclusion Criteria: * History of alcohol/drug abuse * Pregnant or breastfeeding women, unless there are justified and documented needs
Where this trial is running
Negrar, Verona
- IRCCS Sacro Cuore Don Calabria hospital — Negrar, Verona, Italy (RECRUITING)
Study contacts
- Study coordinator: Elvia Malo
- Email: ricerca.clinica@sacrocuore.it
- Phone: +390456014854
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Infections