Status:
RECRUITING
Efficacy and Safety of the CG-100 Intraluminal Bypass Device
Lead Sponsor:
Colospan Ltd.
Conditions:
Rectal Cancer
Rectal Tumor
Eligibility:
All Genders
22-70 years
Phase:
NA
Brief Summary
A randomized trial to assess the safety and efficacy of CG-100 for reducing stoma creation rate in subjects undergoing mesorectal excision.
Detailed Description
A primary diverting stoma is widely used by surgeons in order to bypass the low rectal anastomosis and reduce morbidity associated with anastomotic leaks. Today a stoma is created for all high-risk pa...
Eligibility Criteria
Inclusion Criteria:
- The patient is willing to comply with protocol-specified follow-up evaluations
- 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.
- Patient is diagnosed with colorectal cancer
- 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
- Patients who are scheduled to receive a protective stoma under routine clinical practice during their primary planned operation.
- Patient is scheduled to undergo mechanical bowel preparation
- 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:
- Patient has local or systemic infection at the time of intervention (e.g., peritonitis)
- 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).
- Patients with ASA classification > 3
- Albumin < 30 g/liter
- Patient has a diagnosis of bowel obstruction, bowel strangulation, peritonitis, bowel perforation, ischemic bowel, carcinomatosis or extensively spread inflammatory bowel disease
- Patients has a diagnosis of coagulopathy, thrombocytopenia, immune suppression
- BMI ≥ 40
- Patient is going through another surgical procedure (other than ileostomy, adhesiolysis) during the surgery.
- The patient is currently participating in another investigational drug or device study unless pre-approved by the sponsor.
- Patient has been taking regular systemic/ steroid medication in the last 6 months.
- Patients is taking antimetabolites or antiplatelet agents.
- Patient has preexisting sphincter problems
- Patient has evidence of extensive local disease in the pelvis or has undergone a prior pelvic anastomosis.
- Patients with massive diverticulosis at the sigmoid/descending colon (viewed on preoperative CT)
- Any condition or abnormality which in the opinion of the investigator may jeopardize the patient's safe participation or the quality of the data
- 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.
Key Trial Info
Start Date :
June 23 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 31 2026
Estimated Enrollment :
250 Patients enrolled
Trial Details
Trial ID
NCT04184973
Start Date
June 23 2020
End Date
December 31 2026
Last Update
October 23 2025
Active Locations (14)
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1
University of California Irvine
Orange, California, United States, 92868
2
Kaiser Permanente San Diego medical Center
San Diego, California, United States, 92123
3
Colorado University Anschutz Medical Campus
Aurora, Colorado, United States, 80045
4
University of Louisville
Louisville, Kentucky, United States, 40202