EligibleTrials

Efficacy and Safety of the CG-100 Intraluminal Bypass Device

Recruiting · NCT04184973 · Interventional (participants receive a specific treatment) · Lead sponsor: Colospan Ltd.

View the official record on ClinicalTrials.gov →
Colorectal cancer

Interventions studied

CG-100 intraluminal bypass deviceStoma

What this trial is about

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

Who can take part

Age range
22 Years to 70 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

10 locations listed across 5 US states.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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