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"Cross" Closure for Reconstructing the Perineal Wound of Abdominoperineal Resection (CCRPWAR)

Primary Purpose

Rectal Cancer, Anal Canal Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Traditional Closure
"Cross" closure
Sponsored by
Sixth Affiliated Hospital, Sun Yat-sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rectal Cancer focused on measuring Traditional closure, "Cross" closure, Rectal cancer, Anal canal cancer, Abdominoperineal resection

Eligibility Criteria

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

Inclusion Criteria:

  1. Age: 18-75 years old;
  2. ECOG performance status: 0-2;
  3. Histologically confirmed rectal cancer or anal canal cancer;
  4. Completely resected the primary tumor;
  5. No evidence of distant metastasis;
  6. Tolerable general anesthesia;
  7. Total radiation dose of 45-50 Gy needed if the patient needs to receive routine segmental radiotherapy;
  8. Provision of written informed consent.

Exclusion Criteria:

  1. Emergency surgery required when the patients combined with acute ileus, perforation and hemorrhage;
  2. Extralevator abdominoperineal resection needed;
  3. American Society of Anesthesiologists (ASA) IV or V;
  4. Combined with other tumors;
  5. Severe mental illness;

(7)Serious cardiovascular disease, uncontrolled infections, or other serious uncontrolled concomitant disease; (8)Expectation of lateral lymph node dissection preoperatively

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    Traditional Closure

    "Cross" Closure

    Arm Description

    Patients receive primary closure discontinuously for reconstruction of APR perineal wound

    Patients receive "cross" closure for reconstruction of APR perineal wound

    Outcomes

    Primary Outcome Measures

    Complication rate of perineal wound
    the complications of perineal wound are include wound infection, wound effusion, wound liquefaction, wound dehiscence, seroma or hematoma ,delayed wound healing, presacral or perineal abscess, perineal or pelvic floor hernia

    Secondary Outcome Measures

    Primary wound healing rate
    the Primary wound healing rate within 30 days after operation
    CTCAE grade for complications of perineal wound
    the CTCAE grade for complications of perineal wound within 30 days after surgery
    The incidence of each complication of perineal wound
    The incidence of each complication of perineal wound within 30 days after surgery
    The rate of reoperation
    The rate of reoperation within 30 days after surgery
    The volumes of presacral drainage
    The volumes of presacral drainage within 3, 5, 7 days after surgery
    The volumes of presacral residual cavity hydrops
    The volumes of presacral residual cavity hydrops within 3 and 7 days postoperatively
    The times of dressing change of perineal wound
    The times of dressing change of perineal wound within 3, 5, 7 days after surgery
    Removal time of presacral drainage tube
    Removal time of presacral drainage tube within 30 days after surgery
    Scar scores for perineal wound and evaluation of patients' overall satisfaction
    Scar scores for perineal wound and evaluation of patients' overall satisfaction within 30 days after surgery
    Hospital stay after surgery
    Hospital stay after surgery within 30 days after surgery
    The operation time
    The operation time

    Full Information

    First Posted
    October 26, 2018
    Last Updated
    November 7, 2018
    Sponsor
    Sixth Affiliated Hospital, Sun Yat-sen University
    Collaborators
    First Affiliated Hospital, Sun Yat-Sen University, First Affiliated Hospital of Jinan University, The First Affiliated Hospital of Guangzhou Medical University, Second Affiliated Hospital of Guangzhou Medical University, Southern Medical University, China, Guangdong Provincial Hospital of Traditional Chinese Medicine, Guangzhou First People's Hospital, Affiliated Hospital of Guangdong Medical University, Cancer Institute and Hospital, Chinese Academy of Medical Sciences, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Meizhou People's Hospital, Jieyang People's Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03731754
    Brief Title
    "Cross" Closure for Reconstructing the Perineal Wound of Abdominoperineal Resection
    Acronym
    CCRPWAR
    Official Title
    "Cross" Closure for Reconstructing the Perineal Wound of Abdominoperineal Resection in Rectal and Anal Cancer Patients: a Multi-center, Randomized, Open-Label, Positive, Parallel Controlled Clinical Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2018
    Overall Recruitment Status
    Unknown status
    Study Start Date
    November 20, 2018 (Anticipated)
    Primary Completion Date
    November 20, 2020 (Anticipated)
    Study Completion Date
    December 20, 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Sixth Affiliated Hospital, Sun Yat-sen University
    Collaborators
    First Affiliated Hospital, Sun Yat-Sen University, First Affiliated Hospital of Jinan University, The First Affiliated Hospital of Guangzhou Medical University, Second Affiliated Hospital of Guangzhou Medical University, Southern Medical University, China, Guangdong Provincial Hospital of Traditional Chinese Medicine, Guangzhou First People's Hospital, Affiliated Hospital of Guangdong Medical University, Cancer Institute and Hospital, Chinese Academy of Medical Sciences, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Meizhou People's Hospital, Jieyang People's Hospital

    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
    How to reduce the complications of perineal wound after abdominoperineal resection (APR) has always been a hot topic in the medical field.To reduce the complications of perineal wound and the primary healing of perineal wound must meet the two principles of "unobstructed drainage" and " reduced tension closure".This concept is similar to the concepts of closure of enterostomy in rectal cancer patients. It was reported that use of cross-stitch closure can significantly reduce complications of closure of enterostomy. So the investigator ever used the "cross" closure to reconstruct the perineal wound of APR, which was really decrease the complications of perineal wound. However, more clinical trails was needed to confirm the conclusion.
    Detailed Description
    Perineal wound problems after abdominoperineal resection (APR) for rectal cancer is reported in up to 25%~66% of patients,if the perineum does not heal primarily, the secondary wound healing may prolong hospital stay, may necessitate surgical reintervention, and often requires intensive wound care for several months. Great efforts have been taken to reduce the complications of perineal wound of APR, but the incidence of the perineal wound complications are not effectively decreased. It was reported that one of the most important factors to determine the primary healing of perineal wound is whether the anterior sacral drainage and perineal stump drainage are sufficient and effective or not, which is similar to the concept of closure of enterostomy. Previously, it was reported that "cross" closure is an effective method of skin closure for stoma reversal, which allows increased surgical exposure, reduces suture, smooth drainage, aesthetic healing simplifies wound care, and gives a neat cosmetic result. Therefore, because of the success use of "cross" closure in stoma reversal to reduce the complications of perineal wound, the investigator used the "cross" closure to reconstruct the perineal wound of APR, and it really can decrease the complications of perineal wound. However, more clinical trails are needed to confirm the conclusion.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Rectal Cancer, Anal Canal Cancer
    Keywords
    Traditional closure, "Cross" closure, Rectal cancer, Anal canal cancer, Abdominoperineal resection

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    Traditional Closure
    Arm Type
    Active Comparator
    Arm Description
    Patients receive primary closure discontinuously for reconstruction of APR perineal wound
    Arm Title
    "Cross" Closure
    Arm Type
    Experimental
    Arm Description
    Patients receive "cross" closure for reconstruction of APR perineal wound
    Intervention Type
    Procedure
    Intervention Name(s)
    Traditional Closure
    Intervention Description
    Primary closure discontinuously the perineal wound of APR
    Intervention Type
    Procedure
    Intervention Name(s)
    "Cross" closure
    Intervention Description
    Two triangles of skin in the horizontal direction are excised to enlarge the skin incision, and the tumor resected. Then circumferential subcuticular suture of wound, and with tightening of the circumferential suture, the wound resembles a cross.
    Primary Outcome Measure Information:
    Title
    Complication rate of perineal wound
    Description
    the complications of perineal wound are include wound infection, wound effusion, wound liquefaction, wound dehiscence, seroma or hematoma ,delayed wound healing, presacral or perineal abscess, perineal or pelvic floor hernia
    Time Frame
    Within 30 days after operation
    Secondary Outcome Measure Information:
    Title
    Primary wound healing rate
    Description
    the Primary wound healing rate within 30 days after operation
    Time Frame
    Within 30 days after operation
    Title
    CTCAE grade for complications of perineal wound
    Description
    the CTCAE grade for complications of perineal wound within 30 days after surgery
    Time Frame
    Within 30 days after surgery
    Title
    The incidence of each complication of perineal wound
    Description
    The incidence of each complication of perineal wound within 30 days after surgery
    Time Frame
    Within 30 days after surgery
    Title
    The rate of reoperation
    Description
    The rate of reoperation within 30 days after surgery
    Time Frame
    Within 30 days after surgery
    Title
    The volumes of presacral drainage
    Description
    The volumes of presacral drainage within 3, 5, 7 days after surgery
    Time Frame
    Within 3, 5, 7 days after surgery
    Title
    The volumes of presacral residual cavity hydrops
    Description
    The volumes of presacral residual cavity hydrops within 3 and 7 days postoperatively
    Time Frame
    3 and 7 days postoperatively
    Title
    The times of dressing change of perineal wound
    Description
    The times of dressing change of perineal wound within 3, 5, 7 days after surgery
    Time Frame
    Within 3, 5, 7 days after surgery
    Title
    Removal time of presacral drainage tube
    Description
    Removal time of presacral drainage tube within 30 days after surgery
    Time Frame
    Within 30 days after surgery
    Title
    Scar scores for perineal wound and evaluation of patients' overall satisfaction
    Description
    Scar scores for perineal wound and evaluation of patients' overall satisfaction within 30 days after surgery
    Time Frame
    Within 30 days after surgery
    Title
    Hospital stay after surgery
    Description
    Hospital stay after surgery within 30 days after surgery
    Time Frame
    Within 30 days after surgery
    Title
    The operation time
    Description
    The operation time
    Time Frame
    Intraoperatively

    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: Age: 18-75 years old; ECOG performance status: 0-2; Histologically confirmed rectal cancer or anal canal cancer; Completely resected the primary tumor; No evidence of distant metastasis; Tolerable general anesthesia; Total radiation dose of 45-50 Gy needed if the patient needs to receive routine segmental radiotherapy; Provision of written informed consent. Exclusion Criteria: Emergency surgery required when the patients combined with acute ileus, perforation and hemorrhage; Extralevator abdominoperineal resection needed; American Society of Anesthesiologists (ASA) IV or V; Combined with other tumors; Severe mental illness; (7)Serious cardiovascular disease, uncontrolled infections, or other serious uncontrolled concomitant disease; (8)Expectation of lateral lymph node dissection preoperatively
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Lei Wang, MD, PhD
    Phone
    86-20-38254052
    Email
    leiwangyinhu@126.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Lei Wang, MD, PhD
    Organizational Affiliation
    Sixth Affiliated Hospital, Sun Yat-sen University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    "Cross" Closure for Reconstructing the Perineal Wound of Abdominoperineal Resection

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