Oral Bevacizumab-800CW and Cetuximab-800CW Administration to Detect Early Esophageal Adenocarcinomas

Recruiting Phase 2 Interventional Study
Barrett's Esophagus Without Dysplasia Barrett Oesophagitis With Dysplasia Esophageal Adenocarcinoma
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Prevention
Participants needed
25 (estimated)
Sponsor
University Medical Center Groningen · Other
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About This Trial

Previous studies have confirmed the great potential of quantitative fluorescence molecular endoscopy (qFME) when looking at additional lesion detection initially missed by high-definition white light endoscopy (HD-WLE) for surveillance of Barrett's esophagus.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * BE patients without dysplasia and with suspected/diagnosed low-grade dysplasia (LGD), high-grade dysplasia (HGD) or superficial EAC and planned diagnostic and/or therapeutic endoscopy * Written informed consent is obtained Exclusion Criteria: * Patients under the age of eigh…
Contacts

Wouter B Nagengast, Prof. dr.

+31(0)503615755

w.b.nagengast@umcg.nl

CONTACT