Compression Anastomosis: Initial Clinical Experience With the ColonRingTM
Phase 4
18 Years
90 Years
18 Years
90 Years
Not Enrolling
Both
Colonic Neoplasms, Rectal Neoplasms, Diverticulitis, Inflammatory Bowel Diseases, Rectal Prolapse
Both
Colonic Neoplasms, Rectal Neoplasms, Diverticulitis, Inflammatory Bowel Diseases, Rectal Prolapse
Trial Information
Compression Anastomosis: Initial Clinical Experience With the ColonRingTM
Inclusion Criteria:
- benign and malign lesions of the colon and rectum
Exclusion Criteria:
- advanced peritonitis (putrid, feculent)
Type of Study:
Interventional
Study Design:
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Outcome Measure:
Anastomotic leakage
Outcome Time Frame:
4-8 weeks
Safety Issue:
Yes
Principal Investigator
Friedrich Herbst, MD, FRCS
Investigator Role:
Principal Investigator
Investigator Affiliation:
St John of God Hospital, Vienna
Authority:
Austria: Ethikkommission
Study ID:
CT2
NCT ID:
NCT01056913
Start Date:
October 2008
Completion Date:
September 2010
Related Keywords:
- Colonic Neoplasms
- Rectal Neoplasms
- Diverticulitis
- Inflammatory Bowel Diseases
- Rectal Prolapse
- anastomotic leakage
- bleeding from the anastomotic region
- anastomotic stenosis
- Neoplasms
- Colonic Neoplasms
- Diverticulitis
- Inflammatory Bowel Diseases
- Intestinal Diseases
- Prolapse
- Rectal Neoplasms
- Rectal Prolapse
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