End-to-End Compression Anastomosis for Left-sided Colectomy Endo-CAR Study
Phase 2
Completed
- Conditions
- Colorectal CancerDiverticulitis
- Registration Number
- NCT00497263
- Lead Sponsor
- Niti Medical Technologies Ltd.
- Brief Summary
the purpose of this study is to evaluate the safety and effectiveness of the Niti CAR-device in the creation of colorectal anastomosis
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
- Patient age over 18
- Patient schedule for colonic surgery requiring E-t-E anastomosis
- Patient is able to understand and to sign the Informed Consent Form
Exclusion Criteria
- Patient has known allergy to Nickel
- Patient with bowel obstruction, strangulation, peritonitis, perforation, local or systemic infection
- Patient on regular steroid medication
- Patient with preexisting sphincter problems or evidence of extensive local disease of the pelvis
- Patient following radiation (that compromised the anastomosis)
- Patient who are undergoing a defunctioning stoma
- Patient with contraindication to general anesthesia
- Patient who is currently participating in other clinical trial
- Patient who refuse consent
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method functioning anastomosis & no occurrence of adverse events related to device use during hospitalization and until 3 months after discharge
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University Hospitals Gasthuisberg Leuven
🇧🇪Leuven, Brabant, Belgium