The Feasibility and Safety of Instruments in Transanal Total Mesorectal Excision (TaTME) for Rectal Cancer (FSI-TaTME)
Primary Purpose
Postoperative Complications
Status
Unknown status
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
TaTME with CS-Compact (GelPoint pathway)
Sponsored by
About this trial
This is an interventional treatment trial for Postoperative Complications focused on measuring TaTME, Complications, Instrument
Eligibility Criteria
Inclusion Criteria:
- rectal cancer patients, confirmed by the endoscopic biopsy;
- curative rectal cancer in clinical stage with resectable lesion, the cTNM stage <T3 stage, with comparable tumor size in low or medial rectum.
- patients' general information, 18ys<age<75ys, no restriction in genders, BMI< or =30kg/m2, no presentation of severe chronic diseases (i.e. COPD), WHO classification <2 (Zubrod-ECOG-WHO)
- patients or representatives have agreed and signed the informed consent documents.
Exclusion Criteria:
- have received neo-adjuvant chemotherapy or radiotherapy before operations;
- previous surgery in pelvis
- uncontrollable diseases such as diseases in cardiopulmonary function, chronic bronchitis, severe hepatitis/diabetes/malnutrition/renal function.
- suffer from other malignant diseases, i.e. gastric cancer, liver cancer.
- pregnant, lactation stage.
- metal disorders.
- lacking qualified compliance.
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
TaTME with CS-Compact (GelPoint Path)
Arm Description
Based on newly-designed devices tailored for transanal TME, CS-Compact, GelPoint and Octoport are employed for the clinical applications.
Outcomes
Primary Outcome Measures
Number of participants with post-operative complications
Number of participants with post-operative complications (e.g. numbers of postoperative bleeding, leakage, infections)
Secondary Outcome Measures
3-year disease free survival rate
3-year disease free survival rate (the period after curative treatment without any detection of disease ), the detailed information of 3y-DFS will be obtained by period follow-up of patients by calls and outpatient checking.
3-year overall survival rate
3-year overall survival rate (the survival period after curative treatment ), the detailed information of 3y-OS will be obtained by period follow-up of patients by calls and outpatient checking.
Full Information
NCT ID
NCT02943694
First Posted
October 20, 2016
Last Updated
October 21, 2016
Sponsor
Ruijin Hospital
Collaborators
Shanghai Jiao Tong University School of Medicine
1. Study Identification
Unique Protocol Identification Number
NCT02943694
Brief Title
The Feasibility and Safety of Instruments in Transanal Total Mesorectal Excision (TaTME) for Rectal Cancer
Acronym
FSI-TaTME
Official Title
The Feasibility and Safety of Instruments in Transanal Total Mesorectal Excision (TaTME) for Rectal Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
October 2016
Overall Recruitment Status
Unknown status
Study Start Date
December 2016 (undefined)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ruijin Hospital
Collaborators
Shanghai Jiao Tong University School of Medicine
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Colorectal cancer is one of the leading deadly diseases in the world. Due to the TME (total mesorectal excision) for the last decades, the survival and relapse rate of rectal cancer patients have been considerably improved. However, anatomical limitations in pelvic space hinder the further optimization of surgical treatment Thus, the natural orifice transluminal endoscopic surgery (NOTES) emerges as an alternative surgical strategy. Of note, transanal total mesorectal excision (TaTME) , a new invention based on TME principle, NOTES conception and single port technique, has been prevailing both in West and East nations, with or without the abdominal laparoscopic assistance. Up to date, there are various kinds of instruments and patterns to complete TaTME with comparable clinical outcomes. However, flaws in each instrument remains according to the feedbacks. This study is therefore designed to clinically evaluate the feasibility and safety of the new instruments specifically for TaTME (CS-Compact, GelPoint pathway).
Detailed Description
Rectal cancer comprises the most in colorectal cancer around the world, among which surgery remains the optimal therapeutic intervention. The TME (Total Mesorectal Excision), proposed by Bill Heald, provides novel insights for the eradication of possible disseminated cancer cells and therefore reduces the recurrence and mortality rates. However, either laparoscopic or open TME surgery is limited by the pelvic space and further improvement. For the last decade, the emerging of the natural orifice transluminal endoscopic surgery (NOTES) offers an alternative pattern for rectal cancer surgery, among which, the TaTME (transanal total mesorectal excision) represents the most optimized surgery techniques. Derived from TME, NOTES and modified laparoscopic instruments, TaTME facilitates the dissection process of rectal cancer from caudal to cranial, from indirect to direct vision. TaTME allows for accurate confirmation of resected margin with proper transecting level, better dissection of mesorectum and protection of sphincter, a qualified end-to-end anastomosis and reduced need of endolinear stapler and possible leakage afterwards. However, various kinds of instruments and surgical procedures have been proposed to complete TaTME, all of which have been validated by preclinical and clinical trials in small size. Of note, this study is initiated to apply a suit of instruments specifically designed for TaTME ( GelPoint pathway CS-Compact) and clinically evaluate the feasibility and safety of the new instruments without comparison to other prevailing ones. The CS-Compact and GelPoint pathway has been confirmed both safe and feasible to operate in preclinical trials and clinical trials in western. This study strictly examines the corresponding issues in Chinese rectal cancer patients. The surgeons in our institute have successfully completed the training programs of TaTME in preclinical trials, in animal models and cadavers. Clinical skills and knowledge to safe operations are qualified.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Complications
Keywords
TaTME, Complications, Instrument
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
32 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
TaTME with CS-Compact (GelPoint Path)
Arm Type
Experimental
Arm Description
Based on newly-designed devices tailored for transanal TME, CS-Compact, GelPoint and Octoport are employed for the clinical applications.
Intervention Type
Device
Intervention Name(s)
TaTME with CS-Compact (GelPoint pathway)
Intervention Description
Standard TaTME with circular stapler (Short and straight, CS Compact), designed for extra-corporeal and endo-anal anastomosis procedures.
Primary Outcome Measure Information:
Title
Number of participants with post-operative complications
Description
Number of participants with post-operative complications (e.g. numbers of postoperative bleeding, leakage, infections)
Time Frame
postoperative 30days (hospital-stay time course)
Secondary Outcome Measure Information:
Title
3-year disease free survival rate
Description
3-year disease free survival rate (the period after curative treatment without any detection of disease ), the detailed information of 3y-DFS will be obtained by period follow-up of patients by calls and outpatient checking.
Time Frame
postoperative 3years
Title
3-year overall survival rate
Description
3-year overall survival rate (the survival period after curative treatment ), the detailed information of 3y-OS will be obtained by period follow-up of patients by calls and outpatient checking.
Time Frame
postoperative 3years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
rectal cancer patients, confirmed by the endoscopic biopsy;
curative rectal cancer in clinical stage with resectable lesion, the cTNM stage <T3 stage, with comparable tumor size in low or medial rectum.
patients' general information, 18ys<age<75ys, no restriction in genders, BMI< or =30kg/m2, no presentation of severe chronic diseases (i.e. COPD), WHO classification <2 (Zubrod-ECOG-WHO)
patients or representatives have agreed and signed the informed consent documents.
Exclusion Criteria:
have received neo-adjuvant chemotherapy or radiotherapy before operations;
previous surgery in pelvis
uncontrollable diseases such as diseases in cardiopulmonary function, chronic bronchitis, severe hepatitis/diabetes/malnutrition/renal function.
suffer from other malignant diseases, i.e. gastric cancer, liver cancer.
pregnant, lactation stage.
metal disorders.
lacking qualified compliance.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jing Sun, Ph.D., M.D.
Phone
13524284622
Email
jingsun1982@sina.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Jian-qing YAO, Ph.D.
Phone
13681815601
Email
JIANMARIA@HOTMAIL.COM
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wei-Guo HU, Ph.D., M.D.
Organizational Affiliation
Ruijin Hospital
Official's Role
Study Director
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
24639052
Citation
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Results Reference
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24225001
Citation
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Results Reference
background
PubMed Identifier
2425199
Citation
Heald RJ, Ryall RD. Recurrence and survival after total mesorectal excision for rectal cancer. Lancet. 1986 Jun 28;1(8496):1479-82. doi: 10.1016/s0140-6736(86)91510-2.
Results Reference
background
PubMed Identifier
8094488
Citation
MacFarlane JK, Ryall RD, Heald RJ. Mesorectal excision for rectal cancer. Lancet. 1993 Feb 20;341(8843):457-60. doi: 10.1016/0140-6736(93)90207-w.
Results Reference
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PubMed Identifier
26659246
Citation
McLemore EC, Harnsberger CR, Broderick RC, Leland H, Sylla P, Coker AM, Fuchs HF, Jacobsen GR, Sandler B, Attaluri V, Tsay AT, Wexner SD, Talamini MA, Horgan S. Transanal total mesorectal excision (taTME) for rectal cancer: a training pathway. Surg Endosc. 2016 Sep;30(9):4130-5. doi: 10.1007/s00464-015-4680-1. Epub 2015 Dec 10.
Results Reference
background
PubMed Identifier
22752277
Citation
Telem DA, Han KS, Kim MC, Ajari I, Sohn DK, Woods K, Kapur V, Sbeih MA, Perretta S, Rattner DW, Sylla P. Transanal rectosigmoid resection via natural orifice translumenal endoscopic surgery (NOTES) with total mesorectal excision in a large human cadaver series. Surg Endosc. 2013 Jan;27(1):74-80. doi: 10.1007/s00464-012-2409-y. Epub 2012 Jun 30.
Results Reference
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PubMed Identifier
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Citation
Atallah S, Albert M, Larach S. Transanal minimally invasive surgery: a giant leap forward. Surg Endosc. 2010 Sep;24(9):2200-5. doi: 10.1007/s00464-010-0927-z. Epub 2010 Feb 21.
Results Reference
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PubMed Identifier
27333465
Citation
Kneist W, Hanke L, Kauff DW, Lang H. Surgeons' assessment of internal anal sphincter nerve supply during TaTME - inbetween expectations and reality. Minim Invasive Ther Allied Technol. 2016 Oct;25(5):241-6. doi: 10.1080/13645706.2016.1197269. Epub 2016 Jun 22.
Results Reference
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PubMed Identifier
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Citation
Muratore A, Mellano A, Marsanic P, De Simone M. Transanal total mesorectal excision (taTME) for cancer located in the lower rectum: short- and mid-term results. Eur J Surg Oncol. 2015 Apr;41(4):478-83. doi: 10.1016/j.ejso.2015.01.009. Epub 2015 Jan 17.
Results Reference
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The Feasibility and Safety of Instruments in Transanal Total Mesorectal Excision (TaTME) for Rectal Cancer
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