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NCT05632744 Clinical Trial

Evaluation of CG-100 Intraluminal Bypass Device

Colorectal Cancer Clinical Trial

Official title:
Evaluation of CG-100 Intraluminal Bypass Device

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05632744
Other study ID # CLD-113
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 15, 2023
Est. completion date June 15, 2024

Study information
Verified date February 2024
Source Colospan Ltd.
Contact Shelly Sharon
Phone +972-50-2988415
Email shelly@colospan.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluation of CG-100 Intraluminal Bypass device

Recruitment information / eligibility
Status Recruiting
Enrollment 10
Est. completion date June 15, 2024
Est. primary completion date June 15, 2024
Accepts healthy volunteers No
Gender All
Age group 22 Years to 75 Years
Eligibility Inclusion Criteria (pre-operative): 1. Willing to comply with protocol-specified follow-up evaluations 2. 22-75 (inclusive) years of age at screening 3. Diagnosed with colorectal cancer 4. Has been informed of the nature of the study, agrees to its provisions, and has provided written informed consent

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• CG-100 Intraluminal Bypass Device
Subjects will be treated with the CG-100 Intraluminal Bypass Device

Locations
Country Name City State
Israel Soroka Medical Center Re?ovot

Sponsors (1)
Lead Sponsor Collaborator
Colospan Ltd.

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Safety of the CG-100 Intraluminal Bypass Device Assessment of Serious Adverse Events 10 days
Secondary Safety of the CG-100 Intraluminal Bypass Device Assessment of Serious Adverse Events 4 weeks
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