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PReventive cOlostomy vs Ileostomy in Low anTErior reCTal Resection (PROTECT)

Primary Purpose

Rectal Cancer

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Low anterior resection with protective loop ileostomy
Low anterior resection with protective loop transverse colostomy
Sponsored by
Russian Society of Colorectal Surgeons
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rectal Cancer focused on measuring colostomy, ileostomy, rectal cancer, low anterior resection

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Mid- and low rectal cancer
  • Age ≧ 18
  • TME
  • ASA ≦ 3
  • No previous stoma formation
  • Informed consent for participation

Exclusion Criteria:

  • Patients lost during the follow-up
  • Refusal of the patient from further participation in the study
  • Inability of stoma formation

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    Ileostomy

    Colostomy

    Arm Description

    Loop protective ileostomy as a defunction mean after low anterior resection with D3 lymphnode dissection

    Loop protective transverse colostomy as a defunction mean after low anterior resection with D3 lymphnode dissection

    Outcomes

    Primary Outcome Measures

    The rate of readmissions due to severe dehydratation
    The percentage of patients who were readmitted to the hospital due to dehydration, that could not be managed in outhospital setting

    Secondary Outcome Measures

    Early postoperative complications rate
    The rate of all postoperative complications in early postoperative period after resectional surgery
    Late postoperative complications rate
    The rate of all postoperative complications
    Overall quality of life
    Assessed with patient-reported questionnaire SF-36. A total score in each of 8 sections will be calculated and transformed into a 0-100 scale with a score of zero equivalent to maximum disability and a score of 100 equivalent to no disability
    Time with stoma
    The period of time between initial resectional procedure and closure of protetctive stoma only in patients who had their intestinal stoma reversed
    The rate of early postoperative complications after stoma closure operation
    The rate of early postoperative complications after stoma closure operation

    Full Information

    First Posted
    April 20, 2020
    Last Updated
    April 20, 2020
    Sponsor
    Russian Society of Colorectal Surgeons
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04357171
    Brief Title
    PReventive cOlostomy vs Ileostomy in Low anTErior reCTal Resection
    Acronym
    PROTECT
    Official Title
    Multi-center, Randomized, Parallel-group, Superiority Study to Compare Outcomes of Protective Double-Barrelled Colostomy Versus Protective Double-Barrelled Ileostomy in Low Anterior Resection for Rectal Cancer
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2020
    Overall Recruitment Status
    Completed
    Study Start Date
    January 14, 2012 (Actual)
    Primary Completion Date
    February 2, 2020 (Actual)
    Study Completion Date
    February 2, 2020 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Russian Society of Colorectal Surgeons

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The type of preventive intestinal stoma (colostomy/ileostomy) after low anterior rectal resection rectum is still a debate. This study purpose is to demonstrate that preventive loop ileostomy is characterized by a higher readmission rate caused by dehydration, in comparison with the loop colostomy.
    Detailed Description
    Modern surgery for the rectal cancer is featured by sphincter-preserving operations. It is proved that colorectal anastomosis leakage is severe and, in some cases, lethal complication that reduces quality of life of patients and increases the risk of disease reccurence. The presence of preventive stoma is an effective way to avoid this complication that is why it's included to treatment protocols for the middle and low ampullary rectal cancers is undisputed by the most of surgeons. However, the type of preventive stoma is under discussion yet and remains to be an urgent issue. The majority of large meta-analyzes demonstrates that preventive ileostomy is used more often for the protection of low colorectal anastomoses. In the western countries the preferred method is double barreled ileostomy due to more rapid formation and closure, as well as due to lower rate of stoma-related morbidity. In Russia and CIS countries the double-barreled transverse colostomy is a preferred method of defuction of low colorectal anastomosis due to lower rate of electrolytic disorders and related hospital admissions, along with series of unproven advantages. Presented study will allow to reveal the early and late postoperative morbidity rate and the related hospital re-admissions in real-life clinical practice of Russia from the standpoints of evidence- based medicine, to define indications and contraindications for each type of "low" colorectal anastomosis protection with the least risk for the patient.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Rectal Cancer
    Keywords
    colostomy, ileostomy, rectal cancer, low anterior resection

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    InvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    202 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Ileostomy
    Arm Type
    Active Comparator
    Arm Description
    Loop protective ileostomy as a defunction mean after low anterior resection with D3 lymphnode dissection
    Arm Title
    Colostomy
    Arm Type
    Active Comparator
    Arm Description
    Loop protective transverse colostomy as a defunction mean after low anterior resection with D3 lymphnode dissection
    Intervention Type
    Procedure
    Intervention Name(s)
    Low anterior resection with protective loop ileostomy
    Intervention Description
    Nerve-sparing paraaortic lymph node dissection is performed. The inferior mesenteric artery is divided at 1-2 cm from its origin from the aorta or right below left colic artery. Nerve-sparing total mesorectal excision is performed. Side-to-end sigmoido-rectal anastomosis is created. A loop defunctioning ileostomy is performed.
    Intervention Type
    Procedure
    Intervention Name(s)
    Low anterior resection with protective loop transverse colostomy
    Intervention Description
    Nerve-sparing paraaortic lymph node dissection is performed. The inferior mesenteric artery is divided at 1-2 cm from its origin from the aorta or right below left colic artery. Nerve-sparing total mesorectal excision is performed. Side-to-end sigmoido-rectal anastomosis is created. A loop defunctioning transverse colostomy is performed.
    Primary Outcome Measure Information:
    Title
    The rate of readmissions due to severe dehydratation
    Description
    The percentage of patients who were readmitted to the hospital due to dehydration, that could not be managed in outhospital setting
    Time Frame
    6 weeks
    Secondary Outcome Measure Information:
    Title
    Early postoperative complications rate
    Description
    The rate of all postoperative complications in early postoperative period after resectional surgery
    Time Frame
    30 days after the initial procedure
    Title
    Late postoperative complications rate
    Description
    The rate of all postoperative complications
    Time Frame
    starting on 31st day and within 6 months in late postoperative period after the initial procedure
    Title
    Overall quality of life
    Description
    Assessed with patient-reported questionnaire SF-36. A total score in each of 8 sections will be calculated and transformed into a 0-100 scale with a score of zero equivalent to maximum disability and a score of 100 equivalent to no disability
    Time Frame
    6 and 12 months after the initial procedure
    Title
    Time with stoma
    Description
    The period of time between initial resectional procedure and closure of protetctive stoma only in patients who had their intestinal stoma reversed
    Time Frame
    5 years
    Title
    The rate of early postoperative complications after stoma closure operation
    Description
    The rate of early postoperative complications after stoma closure operation
    Time Frame
    3 months after stoma closure

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    85 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Mid- and low rectal cancer Age ≧ 18 TME ASA ≦ 3 No previous stoma formation Informed consent for participation Exclusion Criteria: Patients lost during the follow-up Refusal of the patient from further participation in the study Inability of stoma formation
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Petr Tsarkov
    Organizational Affiliation
    Clinic of Colorectal and Minimally Invasive Surgery
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Inna Tulina
    Organizational Affiliation
    Clinic of Colorectal and Minimally Invasive Surgery
    Official's Role
    Study Chair

    12. IPD Sharing Statement

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