iSITE: Investigation of Somatic Alterations in Tumours of the Eye

sample collection of surplus samples not needed for diagnostic or pathological requirements

An NHS or CRN staff member will inform patients of the nature and objectives of the study, go through the participant information sheet, highlighting possible risks associated with their participation and reiterate the voluntary nature of this study. Patients will be given opportunities to ask questions pertaining to the study. If the potential participant is still interested in taking part, written informed consent for the study will then be received and a copy of the informed consent will be given to the participant to keep.

Patient will complete in own time. To take place in a routine outpatient clinic appointment

To take place in an outpatient clinic.