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Clinical Trials in Italy / NCT07828665
Recruiting Not applicable

Development of a Duodenal Organoid Model for Host-Intestinal Pathogen Interaction Studies

NCT07828665 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2026-06-09
Last updated
2026-09-18

Condition(s) studied

OrganoidModel Disease

Investigational drug(s) / intervention(s)

Donation of residual biological samples for the development of duodenal organoids.

Donation of residual biological samples for the development of duodenal organoids.: Donation of residual biological samples for the development of duodenal organoids that will be tested for the study of host-intestinal pathogen interactions

Study summary

The goal of this clinical trial is to develop an in vitro model based on human duodenal organoids for the study of interactions between the human intestinal epithelium and enteric pathogens. Patients subjected to surgical removal of a portion of the duodenum for clinical indications, with availability of histologically normal duodenal tissue, will be asked to donate residual biological material for research purposes. The model generation procedure includes isolating intestinal stem cells from duodenal tissue, generating 3D intestinal organoids, expanding and differentiating the organoids, and inducing epithelial polarisation and maturation through air-liquid interface culture. Fully differentiated organoids will be used in in vitro co-culture experiments to assess pathogen viability, as well as the development of host epithelial responses to pathogens or their derivatives. Transcriptomic and proteomic data will also be obtained.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients subjected to surgical removal of a portion of the duodenum for clinical indications, with availability of histologically normal duodenal tissue; * Availability of written informed consent for the use of biological samples for research purposes. Exclusion Criteria: * Absence of informed written consent * Inadequate amount of histologically normal duodenal tissue

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
IRCCS Ospedale Sacro Cuore Don Calabria Negrar Verona Recruiting

More IRCCS Sacro Cuore Don Calabria di Negrar trials in Italy

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07828665 on ClinicalTrials.gov ↗ ← All trials in Italy