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Clinical Trial

Safety and Performance of the CG-100 in Patients Undergoing Colorectal Surgery.

NCT: NCT03423485 · COMPLETED

NCT IDNCT03423485
StatusCOMPLETED
Start Date2018-01-01
Completion2018-12-15
SponsorColospan Ltd. (INDUSTRY)
First posted
Last updated

Brief Summary

The purpose of this study is to evaluate the CG-100 device, a single use, temporary intraluminal bypass device,intended to reduce contact of fecal content with an anastomotic site, following colorectal surgery (open or laparoscopic)

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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