J-Pouch vs Side-to-End Anastomosis After Hand-Assisted Laparoscopic Low Anterior Resection for Rectal Cancer
Primary Purpose
Quality of Life, Fecal Incontinence, Postoperative Complications
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Linear cutter-Circular stapler
Circular stapler
Sponsored by
About this trial
This is an interventional treatment trial for Quality of Life
Eligibility Criteria
Inclusion Criteria:
- patients with rectal cancer which is located up to 12 cm from the dentate line observed with a rigid rectosigmoidoscope
Exclusion Criteria:
- refusal of the patient to participate
- pregnancy,
- previous radiation therapy,
- those have cancers other than adenocarcinoma,
- those planned to have local excision or abdominoperineal resection
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Linear cutter-Circular stapler J pouch
Circular stapler Side-to-end anastomosis
Arm Description
J pouch anal anastomosis after laparoscopic low anterior resection
side to end coloanal anastomosis after laparoscopic low anterior resection
Outcomes
Primary Outcome Measures
Short Form 36 Quality of life Questionnaire
Secondary Outcome Measures
Postoperative complications
Functional outcome measured with Fecal Incontinence Severity Index
Functional outcome measured with Sexual Health Inventory
Functional outcome measured with Overactive Bladder validated 8 scale
Full Information
NCT ID
NCT02627729
First Posted
December 7, 2015
Last Updated
December 9, 2015
Sponsor
Dr. Lutfi Kirdar Kartal Training and Research Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02627729
Brief Title
J-Pouch vs Side-to-End Anastomosis After Hand-Assisted Laparoscopic Low Anterior Resection for Rectal Cancer
Official Title
J-Pouch vs Side-to-End Anastomosis After Hand-Assisted Laparoscopic Low Anterior Resection for Rectal Cancer: Short and Long-Term Outcomes of a Prospective Randomized Trial
Study Type
Interventional
2. Study Status
Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
June 2009 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
February 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dr. Lutfi Kirdar Kartal Training and Research Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Current study aims to analyze the outcomes of j-pouch and side-to-end anastomosis in rectal cancer patients treated with laparoscopic hand-assisted low anterior resection
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Quality of Life, Fecal Incontinence, Postoperative Complications
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care Provider
Allocation
Randomized
Enrollment
74 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Linear cutter-Circular stapler J pouch
Arm Type
Active Comparator
Arm Description
J pouch anal anastomosis after laparoscopic low anterior resection
Arm Title
Circular stapler Side-to-end anastomosis
Arm Type
Active Comparator
Arm Description
side to end coloanal anastomosis after laparoscopic low anterior resection
Intervention Type
Device
Intervention Name(s)
Linear cutter-Circular stapler
Intervention Description
a 5 to 6 cm-long colonic pouch will be created with a 80 mm linear cutting-closing stapler. The anastomosis of j-pouch will be routinely strengthened with 3:0 vicryl sutures. Then, a pouch to anal anastomosis will be performed
Intervention Type
Device
Intervention Name(s)
Circular stapler
Intervention Description
a 5 to 6 cm-long colonic segment will be left at the distal part and a side-to-end anastomosis will be performed.
Primary Outcome Measure Information:
Title
Short Form 36 Quality of life Questionnaire
Time Frame
Change from baseline scores at 4th, 8th and 12th months after stoma reversal
Secondary Outcome Measure Information:
Title
Postoperative complications
Time Frame
30 days postoperatively
Title
Functional outcome measured with Fecal Incontinence Severity Index
Time Frame
Change from baseline scores at 4th, 8th and 12th months after stoma reversal
Title
Functional outcome measured with Sexual Health Inventory
Time Frame
Change from baseline scores at 4th, 8th and 12th months after stoma reversal
Title
Functional outcome measured with Overactive Bladder validated 8 scale
Time Frame
Change from baseline scores at 4th, 8th and 12th months after stoma reversal
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
patients with rectal cancer which is located up to 12 cm from the dentate line observed with a rigid rectosigmoidoscope
Exclusion Criteria:
refusal of the patient to participate
pregnancy,
previous radiation therapy,
those have cancers other than adenocarcinoma,
those planned to have local excision or abdominoperineal resection
12. IPD Sharing Statement
Learn more about this trial
J-Pouch vs Side-to-End Anastomosis After Hand-Assisted Laparoscopic Low Anterior Resection for Rectal Cancer
We'll reach out to this number within 24 hrs