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Clinical Trials in the USA / NCT04184973
Recruiting Not applicable

Efficacy and Safety of the CG-100 Intraluminal Bypass Device

NCT04184973 · tracked via the Priya Life Science USA tracker
Sponsor
Colospan Ltd.
Phase
Not applicable
Started
2020-06-23
Last updated
2026-07-06

Condition(s) studied

Rectal CancerRectal TumorRectal/Anal

Investigational drug(s) / intervention(s)

CG-100 intraluminal bypass deviceStoma

CG-100 intraluminal bypass device: a removable, temporary intraluminal bypass device, developed by Colospan, is designed to safely postpone the creation of a protective stoma until 10 days after surgery only for patients who need it (i.e. have a defect in the anastomosis)

Stoma: Primary protective ileostomy

Study summary

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

Eligibility

Sex
ALL
Min age
22 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: 1. The patient is willing to comply with protocol-specified follow-up evaluations 2. Patient 22-65 years of age at screening, or patient 66-70 years of age at screening with up to one cardiovascular, metabolic or pulmonary comorbidity for which medication is prescribed. 3. Patient is diagnosed with colorectal cancer 4. Patient is scheduled for elective either open, laparoscopic or robotic with mesorectal excision (either abdominal or transanal approach) which will require the creation of an anastomosis, maximally 10 cm from the anal verge 5. Patients who are scheduled to receive a protective stoma under routine clinical practice during their primary planned operation. 6. Patient is scheduled to undergo mechanical bowel preparation 7. The patient has been informed of the nature of the study, agrees to its provisions and has provided written informed consent, approved by the appropriate Medical Ethics Committee (EC) or Institutional Review Board (IRB). Exclusion Criteria: 1. Patient has local or systemic infection at the time of intervention (e.g., peritonitis) 2. Major surgical or interventional procedures within 45 days prior to this study or planned surgical or interventional procedures within 6 months of entry into this study (not including, placement of port for chemotherapy or ureter stent insertion). 3. Patients with ASA classification \> 3 4. Albumin \< 30 g/liter 5. Patient has a diagnosis of bowel obstruction, bowel strangulation, peritonitis, bowel perforation, ischemic bowel, carcinomatosis or extensively spread inflammatory bowel disease 6. Patients has a diagnosis of coagulopathy, thrombocytopenia, immune suppression 7. BMI ≥ 40 8. Patient is going through another surgical procedure (other than ileostomy, adhesiolysis) during the surgery. 9. The patient is currently participating in another investigational drug or device study unless pre-approved by the sponsor. 10. Patient has been taking regular systemic/ steroid medication in the last 6 months. 11. Patients is taking antimetabolites or antiplatelet agents. 12. Patient has preexisting sphincter problems 13. Patient has evidence of extensive local disease in the pelvis or has undergone a prior pelvic anastomosis. 14. Patients with massive diverticulosis at the sigmoid/descending colon (viewed on preoperative CT) 15. Any condition or abnormality which in the opinion of the investigator may jeopardize the patient's safe participation or the quality of the data 16. Pregnant or nursing female patients. Female patients of child-bearing potential must have a negative pregnancy test done within 7 days prior to surgical procedure per site standard test.

Primary outcome measure(s)

Trial sites (10)

FacilityCityRegionStatus
University of California Irvine Irvine California Active Not Recruiting
Kaiser Permanente San Diego medical Center San Diego California Recruiting
Colorado University Anschutz Medical Campus Aurora Colorado Recruiting
Henry Ford Health System Detroit Michigan Recruiting
Lifespan & Brown Surgical Associates Providence Rhode Island Active Not Recruiting
University of Utah Health Salt Lake City Utah Active Not Recruiting
Asklepios Hamburg Germany Recruiting
Soroka University Medical Center Beersheba Israel Recruiting
Humanitas Research Hospital Milan Lombardy Recruiting
CHUV Lausanne Switzerland Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04184973 on ClinicalTrials.gov ↗ ← All trials in the USA