Overview

Investigating the Use of Fluorescent Lectins to Identify Dysplasia and Cancer During Endoscopy and Surgery

Status:
Unknown status
Trial end date:
2018-03-01
Target enrollment:
0
Participant gender:
All
Summary
This is a feasibility study investigating the use of a fluorescently conjugated lectin to identify colorectal dysplasia and cancer during colonoscopy and surgery.
Phase:
Early Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Oxford
Treatments:
Lectins
Criteria
Inclusion Criteria:

- Participant is willing and able to give informed consent for participation in the
study.

- Male or female, aged 18 years or above

- Participants undergoing endoscopic procedures including colonoscopy and flexible
sigmoidoscopy or transanal endoscopic microsurgery (TEMS), including robotic assisted
TEMS

- In the investigator's opinion, is able and willing to comply with all study
requirements

Exclusion Criteria

- Participant who is unable to unwilling to give informed consent

- Female participant who is pregnant, lactating or planning pregnancy during the course
of the trial. If there is an uncertainty regarding whether a woman could be pregnant,
then they will be excluded from the study

- Participants with known egg allergies, ovalbumin allergy and soya allergies