Alternate Title
Basic Trial Information
Objectives
Entry Criteria
Expected Enrollment
Outcomes
Outline
Trial Contact Information
Registry Information
J-Pouch Coloanal Anastomosis Compared With Side-to-End Coloanal Anastomosis After Radiation Therapy and Surgery to Remove the Rectum in Treating Patients With Rectal Adenocarcinoma
| Phase | Type | Status | Age | Sponsor | Protocol IDs |
|---|---|---|---|---|---|
| Phase III | Supportive care | Closed | Over 18 | Other | CKTO-2002-02-POCASTER EU-20247, NCT00070005 |
Objectives
Primary
- Compare functional outcome in patients with mid- or distal rectal adenocarcinoma when treated with J-pouch coloanal anastomosis vs side-to-end coloanal anastomosis after preoperative radiotherapy and total mesorectal excision.
Secondary
- Compare the quality of life of patients treated with these procedures.
- Compare anorectal function in patients treated with these procedures.
Entry Criteria
Disease Characteristics:
- Histologically confirmed adenocarcinoma of the rectum
- T2 or T3 disease
- Disease located in the mid- or distal rectum
- No evidence of metastatic disease
- No preexisting grade III or IV incontinence
- Completed preoperative radiotherapy (5 x 5 Gy) before study entry
Prior/Concurrent Therapy:
Biologic therapy
- Not specified
Chemotherapy
- No prior chemotherapy
Endocrine therapy
- Not specified
Radiotherapy
- See Disease Characteristics
- No prior radiotherapy to the pelvis
Surgery
- No prior colon resection
- No prior anorectal surgery
- No concurrent abdominoperineal resection
Patient Characteristics:
Age
- Over 18
Performance status
- WHO 0-2
Life expectancy
- Not specified
Hematopoietic
- Not specified
Hepatic
- Not specified
Renal
- Not specified
Other
- Working knowledge of the Dutch language
Expected Enrollment
100A minimum of 100 patients (50 per treatment arm) will be accrued for this study.
Outcomes
Primary Outcome(s)Functional outcome as measured by a validated questionnaire
Quality life as measured by a validated questionnaire
Anorectal function as assessed by anorectal manometry and barostat measurements
Outline
This is a randomized, multicenter study. Patients are stratified according to participating center and gender. Patients are randomized to 1 of 2 treatment arms.
- Arm I: Patients undergo total mesorectal excision followed by a J-pouch coloanal anastomosis.
- Arm II: Patients undergo total mesorectal excision followed by a side-to-end coloanal anastomosis.
In both arms, patients receive a temporary ileostomy. The ileostomy is closed after 1 week provided recovery is uneventful and no radiological signs of anastomotic leakage are detected. If early closure is not possible, the ileostomy is closed after 6-8 weeks.
Functional outcome, quality of life, and anorectal function are assessed before surgery and at 4 and 12 months after surgery.
Trial Lead Organizations
Academisch Medisch Centrum at University of Amsterdam
| Roel Bakx, MD, Protocol chair |
| ||
| Registry Information | ||
| Official Title | A Phase III Randomised Study Of J-Pouch Coloanal Anastomosis Versus Side-To-End Coloanal Anastomosis After Preoperative Radiotherapy And Total Mesorectal Excision In Patients With Mid And Distal Rectal Cancer | |
| Trial Start Date | 2002-06-01 | |
| Registered in ClinicalTrials.gov | NCT00070005 | |
| Date Submitted to PDQ | 2003-08-11 | |
| Information Last Verified | 2007-04-10 | |
Note: The purpose of most clinical trials listed in this database is to test new cancer treatments, or new methods of diagnosing, screening, or preventing cancer. Because all potentially harmful side effects are not known before a trial is conducted, dose and schedule modifications may be required for participants if they develop side effects from the treatment or test. The therapy or test described in this clinical trial is intended for use by clinical oncologists in carefully structured settings, and may not prove to be more effective than standard treatment. A responsible investigator associated with this clinical trial should be consulted before using this protocol.
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