Colonoscopy Clinical Trials

Clinical trials related to Colonoscopy Procedure

Multicenter Prospectively Collected Registry of Images and Videos of Colonic Lesions to Develop Artificial Intelligence to Predict Submucosal Invasion

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

It concerns a study in which we wish to collect images and corresponding histological information (microscopic characteristics) in a prospective manner in various European and non-European centers (multicentric). This means that the collection of images is new and happens in the context of a procedure that has not yet been carried out. The relevant procedure will involve a standard colonoscopy during which we wish to collect digital images and videos of large colorectal polyps (colorectal lesions). These images will later be used for the development of a new computer software (artificial intelligence) that is able to predict the histology (microscopic characteristics) and extent of invasion in the intestinal wall (submucosal invasion) all by itself. The latter is one of the goals in the European project ECOPOP in which the sponsor is involved.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Referral for standard or therapeutic colonoscopy

• Digital video material of standard colonoscopy containing at least one colorectal polyp (≥ 10mm) and/or with suspicion of malignancy/submucosal invasion

• Digital images of colorectal polyps ≥ 10mm made during standard colonoscopy and/or with suspicion of malignancy/submucosal invasion Page 11 of 21

• Videos and/or images can be made in white light or any virtual of dye-based enhancement technique

• Colonoscopies performed after IRB approval for this particular study.

• Material collected in adult patients of all sex or race, including pregnant women.

Locations
Other Locations
Belgium
UZ Leuven
RECRUITING
Leuven
Contact Information
Primary
Raf Bisschops, MD
raf.bisschops@uzleuven.be
+32 16 342161
Backup
Anja Luypaerts, CTA
anja.luypaerts@uzleuven.be
+32 16 343357
Time Frame
Start Date: 2022-04-07
Estimated Completion Date: 2030-12
Participants
Target number of participants: 5000
Related Therapeutic Areas
Sponsors
Leads: Universitaire Ziekenhuizen KU Leuven

This content was sourced from clinicaltrials.gov