NL-OMON53297
Not Yet Recruiting
Phase 2
A phase 2 intervention study: Detection of early esophageal neopastic lesions by quantified fluorescence molecular endoscopy using oral and topical administration of bevacizumab-800CW and cetuximab-800CW - Oral fluorescent tracer administration to detect esophageal adenocarcinoma
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- niversitair Medisch Centrum Groningen
- Enrollment
- 25
- Status
- Not Yet Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- BE patients without dysplasia and with suspected/diagnosed LGD, HGD or
- •superficial EAC and planned diagnostic and/or therapeutic endoscopy
- •\- Written informed consent is obtained
Exclusion Criteria
- •\- Patients under the age of eighteen.
- •\- Submucosal and invasive EAC, also defined as EAC with TNM\-classification
- •other than T1\.
- •\- Previous radiation therapy for esophageal cancer
- •\- Known immunoglobulin allergy
- •\- Previous chemotherapy, immunotherapy or related surgery
- •\- Prior bevacizumab or cetuximab treatment
- •\- Medical or psychiatric conditions that compromise the patient\*s ability to
- •give informed consent
- •\- Pregnancy or breast feeding.
Outcomes
Primary Outcomes
Not specified
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