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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
Ruijin Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Postoperative Complications focused on measuring TaTME, Complications, Instrument

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    October 20, 2016
    Last Updated
    October 21, 2016
    Sponsor
    Ruijin Hospital
    Collaborators
    Shanghai Jiao Tong University School of Medicine
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    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
    Siegel R, Desantis C, Jemal A. Colorectal cancer statistics, 2014. CA Cancer J Clin. 2014 Mar-Apr;64(2):104-17. doi: 10.3322/caac.21220. Epub 2014 Mar 17.
    Results Reference
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    PubMed Identifier
    24225001
    Citation
    Brenner H, Kloor M, Pox CP. Colorectal cancer. Lancet. 2014 Apr 26;383(9927):1490-1502. doi: 10.1016/S0140-6736(13)61649-9. Epub 2013 Nov 11.
    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
    background
    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
    background
    PubMed Identifier
    20174935
    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
    background
    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
    background
    PubMed Identifier
    25633642
    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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