Colon cancer, rectal Cancer, colorectal cancer Colon cancer, rectal Cancer, Colorectal cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria:Patients = 18 years oldTNM-stage =T3Scheduled for an open colon or rectal resectionScheduled for HIPEC procedure for colorectal cancerWritten informed consent
Exclusion criteria
Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study:Suspected oversensitivity to light; e.g. patient who has had photodynamic therapyThe use of intravenous fluorescent agents close to the area to be resected
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective of this study is to assess the usability of the HSI laparoscope in terms of quality of measurements. This information will be used to improve and optimize the design of the HSI laparoscope for use in future trials. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary objective of this study is to assess the usability and reception of the data produced by the HSI laparoscope as reported by surgeons; and the surgeons vision of optimal implementation for clinical adoption of the device. | — |
Countries
Netherlands
Contacts
Antoni van Leeuwenhoek (AVL)