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Comparison of Two Types of Surgery in Treating Patients With Rectal Cancer
This study is currently recruiting participants.
Study NCT00007930   Information provided by National Cancer Institute (NCI)
First Received: January 6, 2001   Last Updated: February 6, 2009   History of Changes

January 6, 2001
February 6, 2009
August 1999
 
Local recurrence at 3 years [ Designated as safety issue: No ]
Local recurrence at 3 years
Complete list of historical versions of study NCT00007930 on ClinicalTrials.gov Archive Site
Disease-free and overall survival at 5 years [ Designated as safety issue: No ]
Disease-free and overall survival at 5 years
 
Comparison of Two Types of Surgery in Treating Patients With Rectal Cancer
Randomized Trial of Wide Mesorectal Excision Versus Total Mesorectal Excision for Mid Rectal Cancer

RATIONALE: Surgery to remove the tumor may be an effective treatment for rectal cancer. It is not yet known whether one type of surgery is more effective than another for rectal cancer.

PURPOSE: Randomized phase III trial to compare the effectiveness of two types of surgery in treating patients who have rectal cancer.

OBJECTIVES:

  • Compare local and distant recurrences in patients with mid-rectal cancer treated with wide mesorectal surgical excision with straight colorectal anastomosis versus total mesorectal surgical excision with colonic J pouch coloanal anastomosis.
  • Compare the functional, physiological, and anatomical outcomes in these patients treated with these two surgical procedures.
  • Compare disease-free survival and overall survival in these patients treated with these two surgical procedures.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to treatment center. Patients are randomized to 1 of 2 treatment arms.

  • Arm I: Patients undergo surgical resection with a wide mesorectal excision followed by a straight colorectal anastomosis.
  • Arm II: Patients undergo surgical resection with a total mesorectal excision followed by a colonic J pouch coloanal anastomosis. Patients then receive a temporary ileostomy which is closed 6 weeks later.

Patients are followed at 6 weeks, every 4-6 months for 2 years, every 6 months for 2 years, and then annually thereafter.

PROJECTED ACCRUAL: A minimum of 800 patients (400 per arm) will be accrued for this study.

Phase III
Interventional
Treatment
Colorectal Cancer
  • Procedure: conventional surgery
  • Procedure: laparoscopic surgery
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
800
 
 

DISEASE CHARACTERISTICS:

  • Clinical diagnosis of rectal cancer by colonoscopy or barium enema

    • Distal margin of tumor arises within 9-15 cm from the anal verge as measured by rigid sigmoidoscopy
  • No synchronous multiple adenocarcinomas
  • Candidate for low anterior surgical resection by laparoscopy or conventional open method
  • No evidence of gross metastatic disease
  • No evidence of peritoneal or pelvic metastases

PATIENT CHARACTERISTICS:

Age:

  • 18 and over

Performance status:

  • Not specified

Life expectancy:

  • At least 6 months

Hematopoietic:

  • Not specified

Hepatic:

  • Not specified

Renal:

  • Not specified

Other:

  • No other malignancy within the past 5 years

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Not specified

Chemotherapy:

  • Neoadjuvant or adjuvant chemoradiotherapy allowed

Endocrine therapy:

  • Not specified

Radiotherapy:

  • See Chemotherapy

Surgery:

  • See Disease Characteristics
Both
18 Years and older
No
 
China,   Hong Kong,   Singapore
 
NCT00007930
 
CDR0000068354, NMRC-ICR01, EU-99019
National Medical Research Council (NMRC), Singapore
 
Study Chair: Heah Sieu Min, MD National Cancer Centre, Singapore
National Cancer Institute (NCI)
December 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP