The purpose of this study is: Evaluation of the safety and effectiveness of the Compression Anastomosis Ring (CAR™ 27) device for creation of circular, colorectal anastomoses in previously radiated patients.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
10
Creation of a low colorectal (side or pouch low rectal) compression anastomosis in previously radiated patients
University Hospital, Gasthuisberg
Leuven, Belgium
RECRUITINGTo evaluate for the occurrence of adverse events related to the use of the CAR™ 27 device, include anastomotic leak, bleeding, ring evacuation and strictures at 6 months.
Time frame: Approx. 1 year
Evaluation of the creation of a functioning CAR™ 27 anastomosis in radiated patients
Time frame: Approx. 1 year
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