Clinical Research Directory

Inclusion Criteria: * Age ≥ 18 years - male or female. * Subject/SDM understands and has voluntarily signed and dated Informed Consent Form (ICF). * Subject underwent colorectal surgery with anastomosis. * Subjects must be willing to comply with trial requirements. * Subject has a prophylactic abdominal/pelvic drain after colorectal surgery. Exclusion Criteria: * Subjects/caregiver is unwilling or unable to comply with the requirements of the protocol. * 24 hours or more have passed since the end of the subject's surgery and consent was not attained. * The subject had already developed an anastomotic leak at the time of screening and underwent surgery for treatment of the complication. * Plans that the subject will be discharged in less than 3 days post-surgery. * Subject has reported that they are pregnant. * Subject has a permanent end stoma. * Subject is delirious. * Subject has severe dementia. * Subject was involved in the planning and conduct of the clinical investigation. * Origin™ is not compatible with the drain used on the subject. * Subject and/or caregiver is/are not capable of conducting the calibrations for Stream™ Platform (this can be self-reported or determined by the CRC/HCP/other research staff). * The subject and/or caregiver is/are unable to understand the instructions provided for the management and calibration of Stream™ Platform (this can be self-reported or determined by the CRC/investigator/other research staff).