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Study identifier: NCT04184973 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efficacy and Safety of the CG-100 Intraluminal Bypass Device

Condition: Rectal Cancer · Rectal Tumor · Rectal/Anal  ·  Sponsor: Colospan Ltd.

PhaseNA
Planned participants250
Who can joinAll sexes, 22 Years to 70 Years
Healthy volunteersNo

About this study

A randomized trial to assess the safety and efficacy of CG-100 for reducing stoma creation rate in subjects undergoing mesorectal excision.

This description comes directly from the study's public registry record.

Talk to the study team

Boaz Assaf  ·  +972-9-7672518  ·  boaz@colospan.com

Shelly Sharon, MSc  ·  Shelly@colospan.com

Always discuss trial participation with your own doctor first.

Locations (10)

University of California IrvineIrvine, California, United StatesActive Not Recruiting
Kaiser Permanente San Diego medical CenterSan Diego, California, United StatesRecruiting
Colorado University Anschutz Medical CampusAurora, Colorado, United StatesRecruiting
Henry Ford Health SystemDetroit, Michigan, United StatesRecruiting
Lifespan & Brown Surgical AssociatesProvidence, Rhode Island, United StatesActive Not Recruiting
University of Utah HealthSalt Lake City, Utah, United StatesActive Not Recruiting
AsklepiosHamburg, GermanyRecruiting
Soroka University Medical CenterBeersheba, IsraelRecruiting
Humanitas Research HospitalMilan, Lombardy, ItalyRecruiting
CHUVLausanne, SwitzerlandRecruiting

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Source record: clinicaltrials.gov/study/NCT04184973