Last reviewed · How we verify

NCT04184973

Efficacy and Safety of the CG-100 Intraluminal Bypass Device

Recruiting now NA Last updated 23 October 2025
What this trial tests

NA trial testing CG-100 intraluminal bypass device in Rectal Cancer in 250 participants. Currently enrolling.

Timeline
23 June 2020
Primary endpoint
31 December 2026
31 December 2026

Quick facts

Lead sponsorColospan Ltd.
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeprevention
Enrollment250
Start date23 June 2020
Primary completion31 December 2026
Estimated completion31 December 2026
Sites14 locations across Italy, United States, Israel

Drugs / interventions tested

Conditions studied

Sponsor

Colospan Ltd.

Who can join

Adults 22 to 70, any sex, with Rectal Cancer or Rectal Tumor. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Rectal Cancer

Currently open trials in the same condition.

Other Colospan Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04184973.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing