search
Back to results

Hand Assisted Versus "Pure" Laparoscopic Assisted Proctectomy for Rectal Cancer

Primary Purpose

Rectal Cancer

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
HAL proctectomy
"straight" laparoscopic proctectomy
Hand-assisted laparoscopic proctectomy
SL Proctectomy
Sponsored by
Weill Medical College of Cornell University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rectal Cancer focused on measuring hand assisted laparoscopy, rectal cancer, short term outcomes, straight laparoscopy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age > = 18 years of age
  • Histologically proven rectal cancer
  • Inferior margin of the cancer located within 15 cm from the anal verge as determined by rigid sigmoidoscopy
  • No evidence of distant metastases
  • Childbearing age women with negative pregnancy test
  • Patient is a candidate for elective rectal resection
  • The patient, or their representative, is able to understand the study and is willing to consent to participation in the study.

Exclusion Criteria:

  • Age < 18 years of age
  • Surgically unresectable rectal cancer
  • Patients who will require APR or hand-sewn colo-anal anastomosis
  • ASA class 4 or 5
  • Patients having additional surgical procedures which may have affect recovery
  • Child bearing age women with positive pregnancy test
  • Patients with contraindication for treatment by laparoscopy
  • Patients or their representative who are unable to understand the conditions and objectives of the study

Sites / Locations

  • Sang Lee

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

HAL Proctectomy

SL Proctectomy

Arm Description

Hand-assisted laparoscopic proctectomy

"straight" laparoscopic proctectomy

Outcomes

Primary Outcome Measures

operative time

Secondary Outcome Measures

Adequacy of resection margins
In-hospital mortality and morbidity
urinary and sexual function

Full Information

First Posted
March 31, 2008
Last Updated
January 10, 2019
Sponsor
Weill Medical College of Cornell University
search

1. Study Identification

Unique Protocol Identification Number
NCT00651677
Brief Title
Hand Assisted Versus "Pure" Laparoscopic Assisted Proctectomy for Rectal Cancer
Official Title
A Multicenter Prospective Randomized Study Comparing Hand Assisted Versus "Pure" Laparoscopic Assisted Proctectomy for Rectal Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
April 2011
Overall Recruitment Status
Withdrawn
Why Stopped
funding issues
Study Start Date
April 2011 (undefined)
Primary Completion Date
November 2012 (Anticipated)
Study Completion Date
December 2012 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Weill Medical College of Cornell University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
We hypothesize that hand-assisted laparoscopy will overcome technical difficulties related to pure laparoscopic rectal surgery and allow surgeons to expand application of laparoscopic techniques to treating patients with rectal cancer. In this study, we plan to randomly assign patients diagnosed with rectal cancer to undergo either "standard" laparoscopic surgery or hand-assisted laparoscopic surgery. We will then compare both peri-operative and long-term outcomes of patients.
Detailed Description
Compared to traditional open surgery, laparoscopic surgery for colon cancer results in short-term benefits such as less pain, shorter length of stay, and faster return of bowel function while maintaining equivalent oncologic outcomes. For this reason, increasing numbers of colon cancer patients are undergoing laparoscopic surgery.1-3 Similarly, there are many potential benefits to performing rectal surgery laparoscopically. Although not well documented, laparoscopic rectal surgery is under active study and may result in the usual short-term benefits associated with laparoscopic surgery. In addition, compared to open surgery, laparoscopy can provide unprecedented, unobstructed views of the rectal dissection planes even in a patient with narrow pelvis, not only for the surgeon but to the entire surgical team. Magnified views of the surgical planes allow precise and sharp dissection. The pneumoperitoneum can also help open the planes for mobilization of the mesorectum. Despite these potential advantages, adoption of laparoscopic rectal surgery has been limited for many reasons. Although there are now several prospective randomized trials demonstrating safety and benefits associated with laparoscopic colon cancer surgery, the same benefits have not yet been clearly demonstrated for laparoscopic rectal cancer surgery.1-3 In addition, concerns about inadequate oncologic rectal dissection, anastomotic complications, and technical challenges have limited wide adaptation of laparoscopic rectal surgery.4,5 In efforts to retain the benefits of laparoscopic surgery while not compromising oncologic rectal dissection, others have advocated performing hybrid procedures in which colonic portion of the surgery is performed using the "pure" laparoscopic technique and rectal dissection is performed open through a limited low midline or Pfannestiel (low transverse) incision.6 Hand-assisted laparoscopic surgery is a technique in which the surgeon places a hand into the abdomen through an airtight access device while performing laparoscopic surgery. By placing a hand into the abdomen during laparoscopy, surgeons retain their abilities to manually retract, expose, and manually dissect, which are lost in pure laparoscopic surgery. Retention of these abilities can significantly expedite the operation. In fact, several studies have demonstrated that hand-assisted laparoscopic colon surgery results in significantly shorter operative time and less conversion to open surgery while maintain similar short-term outcomes compared to "pure" laparoscopic technique.7-9 In rectal surgery for cancer, sigmoid colon, left colon, and splenic flexure need to be mobilized in order to allow tension free anastomosis between the colon and the residual rectum. In laparoscopic proctectomy, HALS compared to SLS technique may therefore, result in shorter operative time based on colonic portion of the operation alone. One of the technical hurdles in performing laparoscopic rectal dissection is exposure and retraction of the rectum. As one dissects down to the distal rectum, especially in patients with narrow pelvis, crowding and clashing of instruments can result in poor exposure and dissection. The only prospective randomized trial comparing results of open vs. laparoscopic surgery to include rectal cancer is CLASICC trial.3 It reported an increased circumferentially positive margin of cancer following laparoscopic rectal resection with twice as many patients in the laparoscopic group (12 %) having an involved margin as in the open group (6 %). This increased radial margin may be related to difficulty in retraction and exposure. In HALS, rectal exposure and dissection can be either performed directly through the incision using the open techniques or laparoscopically with manual assistance. This may result in equivalent oncologic outcomes as the open surgery but with shorter operative time compared to SLS technique. A further challenge in laparoscopic rectal surgery is localization of the tumor, which is less of an issue in colon cancer where the tumor is easily visible or tattooed preoperatively. This is not possible for rectal cancer, which can pose a problem in both dissection and safe division of the rectum. Without tactile sensation it can be difficult to be sure that the stapler is below the tumor. Hand assisted laparoscopic surgery allows preservation of tactile sensation and therefore circumvent the above problem. The next step following mobilization of the rectum is division of the rectum and anastomosis. This poses a challenge for the laparoscopic surgeon for several reasons. The current laparoscopic stapling devices angulate to a maximum of 65 o making horizontal division of the rectum difficult. Morin et al reported a leak rate of 17 % below 12 cm from the anal verge and as high as 25 % in those who were not diverted following laparoscopic rectal surgery.4 Leroy et al reported a similar leak rate of 20 % in cancers below 15 cm following laparoscopic rectal surgery.5 Comparatively higher leak rates after laparoscopic rectal surgery may be related to limitations in currently available laparoscopic surgical staplers. By performing distal rectal division through the incision by using the open surgical staplers, hand-assisted laparoscopic rectal surgery may result in lower anastomotic leakage rate. We hypothesize that hand-assisted laparoscopy may result in shorter operative time while retaining the benefits associated with laparoscopic surgery. In this study, we plan to randomly assign patients diagnosed with rectal cancer to undergo either "standard" laparoscopic surgery or hand-assisted laparoscopic surgery. We will then compare both peri-operative and long-term outcomes of patients. If our hypothesis is true, hand assisted laparoscopic approach to rectal surgery may be preferable to standard laparoscopic surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rectal Cancer
Keywords
hand assisted laparoscopy, rectal cancer, short term outcomes, straight laparoscopy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HAL Proctectomy
Arm Type
Active Comparator
Arm Description
Hand-assisted laparoscopic proctectomy
Arm Title
SL Proctectomy
Arm Type
Active Comparator
Arm Description
"straight" laparoscopic proctectomy
Intervention Type
Procedure
Intervention Name(s)
HAL proctectomy
Other Intervention Name(s)
Gelport
Intervention Description
Hand-assisted laparoscopic proctectomy
Intervention Type
Procedure
Intervention Name(s)
"straight" laparoscopic proctectomy
Intervention Description
"straight" laparoscopic proctectomy
Intervention Type
Procedure
Intervention Name(s)
Hand-assisted laparoscopic proctectomy
Other Intervention Name(s)
Gelport
Intervention Description
hand-assisted laparoscopic proctectomy
Intervention Type
Procedure
Intervention Name(s)
SL Proctectomy
Intervention Description
Straight laparoscopic proctectomy
Primary Outcome Measure Information:
Title
operative time
Time Frame
post-operative
Secondary Outcome Measure Information:
Title
Adequacy of resection margins
Time Frame
post-operative
Title
In-hospital mortality and morbidity
Time Frame
during hospitalization
Title
urinary and sexual function
Time Frame
preoperative and 3-6 months postop

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > = 18 years of age Histologically proven rectal cancer Inferior margin of the cancer located within 15 cm from the anal verge as determined by rigid sigmoidoscopy No evidence of distant metastases Childbearing age women with negative pregnancy test Patient is a candidate for elective rectal resection The patient, or their representative, is able to understand the study and is willing to consent to participation in the study. Exclusion Criteria: Age < 18 years of age Surgically unresectable rectal cancer Patients who will require APR or hand-sewn colo-anal anastomosis ASA class 4 or 5 Patients having additional surgical procedures which may have affect recovery Child bearing age women with positive pregnancy test Patients with contraindication for treatment by laparoscopy Patients or their representative who are unable to understand the conditions and objectives of the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sang W Lee, MD
Organizational Affiliation
Weill Medical College of Cornell University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sang Lee
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Hand Assisted Versus "Pure" Laparoscopic Assisted Proctectomy for Rectal Cancer

We'll reach out to this number within 24 hrs