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Endoscopic Submucosal Dissection Versus Laparoscopic Resection for Early Colorectal Neoplasms

Primary Purpose

Colorectal Neoplasms

Status
Unknown status
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Endoscopic submucosal dissection
Laparoscopic resection
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colorectal Neoplasms focused on measuring Early colorectal neoplasms

Eligibility Criteria

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

Inclusion Criteria:

  • Patients diagnosed with early colorectal neoplasms >/= 2 cm in size in the colon or upper rectum (>/= 15 cm above the anal verge) that are deemed not feasible for en bloc resection with conventional polypectomy or EMR as judged by 2 experienced endoscopists,
  • Age of patients >18 years,
  • Patients with American Society of Anesthesiologists (ASA) grading I-III,
  • Informed consent available

Exclusion Criteria:

  • Presence of endoscopic signs of massive submucosal invasion (including excavated/depressed morphology or Kudo's pit pattern Type V),
  • Endosonographic evidence of deep invasion,
  • Unfavorable histopathologic features on biopsy (including mucinous cancer, poor differentiation, and gross submucosal invasion),
  • Patients with other synchronous colorectal neoplasms in addition to the index neoplasm that are not amenable to complete endoscopic removal, neoplasms occupying more than half circumference of the colonic wall,
  • Patients with recurrence from previous endoscopic mucosal resection or ESD,
  • Patients with known metastatic disease,
  • Patients with previous history of abdominal surgery, and patients with non-correctable coagulopathy

Sites / Locations

  • Prince of Wales Hospital, The Chinese University of Hong KongRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Endoscopic submucosal dissection

Laparoscopic resection

Arm Description

Outcomes

Primary Outcome Measures

Short-term morbidity

Secondary Outcome Measures

Systemic cytokine and C-reactive protein levels
Measured at 2 hours, 8 hours, 24 hours, 48 hours, and 5 days after ESD/surgery
Post-ESD/surgery recovery
Time to resume normal diet, time to walk independently, and duration of hospital stay
Quality of life
Measured by Short Form-36 (SF-36) and European Organization for Research and Treatment of Cancer (EORTC) QLQ-C30 questionnaires at 3, 6, 9, and 12 months after ESD/surgery
Direct and indirect medical costs
Local recurrence

Full Information

First Posted
April 26, 2010
Last Updated
February 10, 2014
Sponsor
Chinese University of Hong Kong
Collaborators
United Christian Hospital, Queen Elizabeth Hospital, Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT01112046
Brief Title
Endoscopic Submucosal Dissection Versus Laparoscopic Resection for Early Colorectal Neoplasms
Official Title
Endoscopic Submucosal Dissection Versus Laparoscopic Resection for Early Colorectal Neoplasms: A Prospective Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2014
Overall Recruitment Status
Unknown status
Study Start Date
April 2010 (undefined)
Primary Completion Date
April 2015 (Anticipated)
Study Completion Date
April 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
Collaborators
United Christian Hospital, Queen Elizabeth Hospital, Hong Kong

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a prospective randomized trial that aimed to compare the short-term clinical outcomes and systemic inflammatory/cytokine responses of endoscopic submucosal dissection versus laparoscopic resection for early colorectal neoplasms that are not amenable to en bloc endoscopic resection with conventional techniques.
Detailed Description
Colonoscopy plays an increasingly important role in the diagnosis and treatment of colorectal pathologies. The recent progress in endoscopic technologies and interest in colorectal cancer screening have enabled the diagnosis of a larger number of early colorectal neoplasms, including benign polyps and early cancers. Colonoscopic polypectomy remains the cornerstone of therapy for the majority of colorectal polyps and helps prevent colorectal cancer. However, if colorectal neoplasms are too large or cannot be removed "en bloc" endoscopically, operative procedures are required to reduce risks of incomplete removal and local recurrence. Laparoscopic resection represents a minimally invasive alternative for treating colorectal neoplasms that are not amenable to en bloc endoscopic resection. However, laparoscopic surgery has to be done under general anesthesia, is associated with operative morbidity, and is expensive. Endoscopic submucosal dissection (ESD) is a revolutionary endoscopic procedure that enables en bloc resection of large gastrointestinal tumors, irrespective of the size of the lesion. ESD, which was pioneered in Japan for the treatment of early gastric neoplasms, has now been successfully applied to the colon and rectum. ESD has been shown by recent studies to be a safe and effective resection technique for large early colorectal neoplasms. However, no report can be found in the literature comparing ESD and laparoscopic resection for early colorectal neoplasms that are not amenable to en bloc endoscopic resection with conventional techniques. Furthermore, it remains unclear whether ESD is less invasive than laparoscopic surgery in terms of systemic inflammatory and cytokine responses, and all these may have implications for cancer recurrence. We propose to conduct a prospective randomized trial to compare the short-term clinical outcomes and systemic inflammatory/cytokine responses of ESD versus laparoscopic resection for early colorectal neoplasms that are not amenable to en bloc endoscopic resection with conventional techniques. The overall costs of the two therapeutic approaches will also be compared. Findings of this proposed project may provide evidence-based clarification of the efficacy and safety of ESD in treating early colorectal neoplasms. We hypothesize that ESD is associated with lower morbidity, earlier recovery, shorter hospital stay, and lower costs when compared with laparoscopic resection. A faster recovery and earlier discharge after ESD may reduce financial burden to the hospital and health care system. The results of this proposed project may have a significant impact on the future treatment strategy for early colorectal neoplasms, and may provide new insights into the systemic inflammatory responses of ESD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Neoplasms
Keywords
Early colorectal neoplasms

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
124 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Endoscopic submucosal dissection
Arm Type
Experimental
Arm Title
Laparoscopic resection
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
Endoscopic submucosal dissection
Other Intervention Name(s)
ESD
Intervention Description
Endoscopic treatment (performed under conscious sedation) using specific endoscopic knives
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic resection
Intervention Description
Surgical treatment performed under general anesthesia
Primary Outcome Measure Information:
Title
Short-term morbidity
Time Frame
Up to 1 month
Secondary Outcome Measure Information:
Title
Systemic cytokine and C-reactive protein levels
Description
Measured at 2 hours, 8 hours, 24 hours, 48 hours, and 5 days after ESD/surgery
Time Frame
Up to 5 days
Title
Post-ESD/surgery recovery
Description
Time to resume normal diet, time to walk independently, and duration of hospital stay
Time Frame
Up to 1 month
Title
Quality of life
Description
Measured by Short Form-36 (SF-36) and European Organization for Research and Treatment of Cancer (EORTC) QLQ-C30 questionnaires at 3, 6, 9, and 12 months after ESD/surgery
Time Frame
Up to 1 year
Title
Direct and indirect medical costs
Time Frame
Up to 1 year
Title
Local recurrence
Time Frame
Within 5 years after ESD/surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients diagnosed with early colorectal neoplasms >/= 2 cm in size in the colon or upper rectum (>/= 15 cm above the anal verge) that are deemed not feasible for en bloc resection with conventional polypectomy or EMR as judged by 2 experienced endoscopists, Age of patients >18 years, Patients with American Society of Anesthesiologists (ASA) grading I-III, Informed consent available Exclusion Criteria: Presence of endoscopic signs of massive submucosal invasion (including excavated/depressed morphology or Kudo's pit pattern Type V), Endosonographic evidence of deep invasion, Unfavorable histopathologic features on biopsy (including mucinous cancer, poor differentiation, and gross submucosal invasion), Patients with other synchronous colorectal neoplasms in addition to the index neoplasm that are not amenable to complete endoscopic removal, neoplasms occupying more than half circumference of the colonic wall, Patients with recurrence from previous endoscopic mucosal resection or ESD, Patients with known metastatic disease, Patients with previous history of abdominal surgery, and patients with non-correctable coagulopathy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Simon SM Ng, MD
Phone
(852) 2632 1495
Email
simonng@surgery.cuhk.edu.hk
First Name & Middle Initial & Last Name or Official Title & Degree
Sophie SF Hon, MD
Phone
(852) 2632 1495
Email
honsf@surgery.cuhk.edu.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Simon SM Ng, MD
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Prince of Wales Hospital, The Chinese University of Hong Kong
City
Hong Kong
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Simon SM Ng, MD
Phone
(852) 2632 1495
Email
simonng@surgery.cuhk.edu.hk
First Name & Middle Initial & Last Name & Degree
Simon SM Ng, MD
First Name & Middle Initial & Last Name & Degree
Philip WY Chiu, MD
First Name & Middle Initial & Last Name & Degree
Sophie SF Hon, MD

12. IPD Sharing Statement

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Endoscopic Submucosal Dissection Versus Laparoscopic Resection for Early Colorectal Neoplasms

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