Collection of endoscopic images and data from procedures at UZ Gent
Prospective Collection of Endoscopic and Histopathologic Data from Endoscopic Procedures Performed in UZ Gent
This study is collecting images and information from endoscopic procedures to better understand tough-to-manage lesions and improve care for patients.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 510 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Ghent Academic / other |
| Locations | 1 site (Ghent, East Flanders) |
| Trial ID | NCT06467929 on ClinicalTrials.gov |
What this trial studies
This observational study aims to collect high-quality images and videos of lesions encountered during endoscopic procedures, along with detailed histopathological data. The study focuses on documenting various lesions, particularly large sessile lesions, which are challenging to manage and have a higher risk of advanced histology. By creating a comprehensive database, the study seeks to enhance understanding of endoscopic techniques and outcomes, ultimately improving patient care. All data collection will adhere to GDPR regulations to ensure patient confidentiality.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who are referred for surveillance, diagnostic, or therapeutic endoscopy.
Not a fit: Patients under 18 years old or those with contraindications to endoscopic procedures will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve the management and outcomes of patients undergoing endoscopic procedures by providing valuable insights into lesion characteristics and treatment efficacy.
How similar studies have performed: Previous prospective studies have shown success in improving the management of large sessile lesions through endoscopic techniques, indicating that this approach is supported by existing evidence.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age =\> 18 years * Referral for a surveillance, diagnostic or therapeutic endoscopy * Digital video material of the endoscopic procedure * Digital images of the endoscopic procedure * Videos and/or images can be made in white light or any virtual of dye-based enhancement technique * Endoscopic procedures performed after IRB approval for this study * Material collected in adult patients of all sex or race, including pregnant women Exclusion Criteria: * Age \< 18 years * Any contraindication to undergo an endoscopic procedure * Patient did not sign informed consent
Where this trial is running
Ghent, East Flanders
- University Hospital Ghent — Ghent, East Flanders, Belgium (Recruiting)
Study contacts
- Principal investigator: David Tate, Doctor — UZ Gent
- Study coordinator: Karolien Haenebalcke
- Email: karolien.haenebalcke@uzgent.be
- Phone: 93321063
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.