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PE-Bacon for Late Complications of Chronic Radiation-induced Rectal Injury (PE-Bacon)

Primary Purpose

Chronic Radiation Injury

Status
Not yet recruiting
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Parks surgery
PE-Bacon surgery
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 Chronic Radiation Injury focused on measuring PE-Bacon, Parks, complication

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: 1. Patients aged 18-70 years; 2. Patients with Eastern Cooperative Oncology Group (ECOG) physical condition score of 0-2; 3. Patients with previous pathological diagnosis of pelvic tumors (Gynecology, prostate, urinary system); 4. Patients with a history of pelvic radiotherapy, at least 6 months from the end of the last radiotherapy; 5. Patients without recurrence or metastasis of primary tumor; 6. The late complications of CRII patients, such as deep rectal ulcer (VRS score >=3), rectal sigmoid colon stenosis, obstruction, chronic perforation, rectal necrosis, rectovaginal fistula, intractable anal pain caused by rectal lesions, intractable rectal bleeding which is still difficult to be relieved by stoma operation, and patients who need sigmoid colorectal resection; 7. Patients who can tolerate general anesthesia; 8. The subjects and their families are able to understand the study plan, willing to participate and sign the informed consent. Exclusion Criteria: 1. Patients with acute intestinal obstruction, acute intestinal perforation and intestinal hemorrhage who need emergency operation; 2. Patients with severe pelvic adhesion and frozen pelvis; 3. Patients with unstable primary tumor or tumor in other parts; 4. Patients who need to undergo combined organ resection; 5. Patients with a history of sigmoidostomy; 6. American society of anesthesiologists (ASA) level IV to V; 7. Patients with serious mental illness; 8. Pregnant or lactating women; 9. Patients with serious cardiovascular disease, uncontrollable infection, or other uncontrollable combined diseases.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Other

    Experimental

    Arm Label

    Parks surgery group

    PE-Bacon surgery group

    Arm Description

    The CRII patients received Parks surgery

    The CRII patients received PE-Bacon surgery

    Outcomes

    Primary Outcome Measures

    Ostomy reversal rate within 1 year after surgery
    Ostomy reversal rate within 1 year after surgery
    Incidence of anastomotic leakage within 6 months after surgery
    Incidence of anastomotic leakage within 6 months after surgery

    Secondary Outcome Measures

    Ostomy reversal rate within 2 years after surgery
    Ostomy reversal rate within 2 years after surgery
    Ostomy reversal rate within 3 years after surgery
    Ostomy reversal rate within 3 years after surgery
    Incidence of anastomotic leakage within 1 year after surgery
    Incidence of anastomotic leakage within 1 year after surgery
    Incidence of anastomotic leakage within 2 years after surgery
    Incidence of anastomotic leakage within 2 years after surgery
    Incidence of anastomotic leakage within 3 years after surgery
    Incidence of anastomotic leakage within 3 years after surgery
    Incidence of anastomotic stricture within 6 months after surgery
    Incidence of anastomotic stricture within 6 months after surgery
    Incidence of anastomotic stricture within 1 year after surgery
    Incidence of anastomotic stricture within 1 year after surgery
    Incidence of anastomotic stricture within 2 years after surgery
    Incidence of anastomotic stricture within 2 years after surgery
    Incidence of anastomotic stricture within 3 years after surgery
    Incidence of anastomotic stricture within 3 years after surgery
    Incidence of severe intestinal dysfunction at 1 year after ostomy reversal
    Incidence of severe intestinal dysfunction at 1 year after ostomy reversal
    Incidence of severe intestinal dysfunction at 2 years after ostomy reversal
    Incidence of severe intestinal dysfunction at 2 years after ostomy reversal
    Incidence of severe intestinal dysfunction at 3 years after ostomy reversal
    Incidence of severe intestinal dysfunction at 3 years after ostomy reversal
    Quality of life at 1 year after ostomy reversal
    Quality of life at 1 year after ostomy reversal
    Quality of life at 2 years after ostomy reversal
    Quality of life at 2 years after ostomy reversal
    Quality of life at 3 years after ostomy reversal
    Quality of life at 3 years after ostomy reversal

    Full Information

    First Posted
    September 26, 2022
    Last Updated
    November 2, 2022
    Sponsor
    Sixth Affiliated Hospital, Sun Yat-sen University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05607927
    Brief Title
    PE-Bacon for Late Complications of Chronic Radiation-induced Rectal Injury
    Acronym
    PE-Bacon
    Official Title
    Laparoscopic Proximally Extended Colorectal Resection With Two-Stage Turnbull-Cutait Pull-Through Coloanal Anastomosis for Late Complications of Chronic Radiation-induced Rectal Injury: A Prospective, Multicenter, Randomized Controlled Clinical Trail
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    November 20, 2022 (Anticipated)
    Primary Completion Date
    August 30, 2025 (Anticipated)
    Study Completion Date
    August 30, 2028 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Sixth Affiliated Hospital, Sun Yat-sen University

    4. Oversight

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

    5. Study Description

    Brief Summary
    Chronic radiation-induced injury (CRII) is a common complication after radiation therapy for pelvic malignancies. Resection surgery could be an optimal surgical approach when CRII is complicated by late complications. However, because of high incidence of postoperative complications like anastomotic leakage rate and mortality, doctors try to avoid performing surgical resection. In addition, there is sparse agreement on the types of surgery. Previous study proved that anastomosis with at least one end of bowel without radiation damage can greatly reduce postoperative anastomotic leakage rate and mortality. And in Bacon surgery, primary anastomosis is not performed, and the anastomotic tension markedly reduced and the blood supply of anastomosis can be judged intuitively to improve the quality of anastomosis in the second stage of intestinal anastomosis to decrease the anastomotic leakage rate. Combining the advantages of proximally extended resection and two-stage anastomosis could minimize potential complications and maximize the therapeutic efficacy in theory, and a small sample prospective clinical study by the investigator have already preliminarily confirmed it. The investigator has also preliminarily proved that Parks surgery is safe and feasible for the treatment of late complications of CRII. Therefore, this study aims to observe the safety and effectiveness of PE-Bacon surgery with Parks surgery as a control, in order to select more optimal surgical methods and provide a high-level evidence-based medical basis for patients with late complications of CRII.
    Detailed Description
    Chronic radiation-induced injury (CRII) is a common complication after radiation therapy for pelvic malignancies. Compared with diversion surgery, resection surgery removes the damaged tissue completely to avoid the risks of recurrence and improve patients' outcome. Hence, resection surgery could be an optimal surgical approach when CRII is complicated by late complications. However, because of high incidence of postoperative complications like anastomotic leakage rate and mortality, doctors try to avoid performing surgical resection. In addition, there is sparse agreement on the types of surgery. With the advances of surgical techniques and perioperative care, the morbidity and mortality of resection surgery has been decreased significantly. In addition, previous study proved that anastomosis with at least one end of bowel without radiation damage can greatly reduce postoperative anastomotic leakage rate and mortality. And in Bacon surgery, primary anastomosis is not performed, and the anastomotic tension markedly reduced and the blood supply of anastomosis can be judged intuitively to improve the quality of anastomosis in the second stage of intestinal anastomosis to decrease the anastomotic leakage rate. Combining the advantages of proximally extended resection and two-stage anastomosis could minimize potential complications and maximize the therapeutic efficacy in theory, and a small sample prospective clinical study by the investigator have already preliminarily confirmed it. And the investigator has also preliminarily proved that Parks surgery is safe and feasible for the treatment of late complications of CRII. Therefore, this study aims to observe the safety and effectiveness of PE-Bacon surgery with Parks surgery as a control, in order to select more optimal surgical methods and provide a high-level evidence-based medical basis for patients with late complications of CRII.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Chronic Radiation Injury
    Keywords
    PE-Bacon, Parks, complication

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    Parks surgery group
    Arm Type
    Other
    Arm Description
    The CRII patients received Parks surgery
    Arm Title
    PE-Bacon surgery group
    Arm Type
    Experimental
    Arm Description
    The CRII patients received PE-Bacon surgery
    Intervention Type
    Procedure
    Intervention Name(s)
    Parks surgery
    Intervention Description
    Parks surgery
    Intervention Type
    Procedure
    Intervention Name(s)
    PE-Bacon surgery
    Intervention Description
    PE-Bacon surgery
    Primary Outcome Measure Information:
    Title
    Ostomy reversal rate within 1 year after surgery
    Description
    Ostomy reversal rate within 1 year after surgery
    Time Frame
    1 year after surgery
    Title
    Incidence of anastomotic leakage within 6 months after surgery
    Description
    Incidence of anastomotic leakage within 6 months after surgery
    Time Frame
    6 months after surgery
    Secondary Outcome Measure Information:
    Title
    Ostomy reversal rate within 2 years after surgery
    Description
    Ostomy reversal rate within 2 years after surgery
    Time Frame
    2 years after surgery
    Title
    Ostomy reversal rate within 3 years after surgery
    Description
    Ostomy reversal rate within 3 years after surgery
    Time Frame
    3 years after surgery
    Title
    Incidence of anastomotic leakage within 1 year after surgery
    Description
    Incidence of anastomotic leakage within 1 year after surgery
    Time Frame
    1 year after surgery
    Title
    Incidence of anastomotic leakage within 2 years after surgery
    Description
    Incidence of anastomotic leakage within 2 years after surgery
    Time Frame
    2 years after surgery
    Title
    Incidence of anastomotic leakage within 3 years after surgery
    Description
    Incidence of anastomotic leakage within 3 years after surgery
    Time Frame
    3 years after surgery
    Title
    Incidence of anastomotic stricture within 6 months after surgery
    Description
    Incidence of anastomotic stricture within 6 months after surgery
    Time Frame
    6 months after surgery
    Title
    Incidence of anastomotic stricture within 1 year after surgery
    Description
    Incidence of anastomotic stricture within 1 year after surgery
    Time Frame
    1 year after surgery
    Title
    Incidence of anastomotic stricture within 2 years after surgery
    Description
    Incidence of anastomotic stricture within 2 years after surgery
    Time Frame
    2 years after surgery
    Title
    Incidence of anastomotic stricture within 3 years after surgery
    Description
    Incidence of anastomotic stricture within 3 years after surgery
    Time Frame
    3 years after surgery
    Title
    Incidence of severe intestinal dysfunction at 1 year after ostomy reversal
    Description
    Incidence of severe intestinal dysfunction at 1 year after ostomy reversal
    Time Frame
    1 year after ostomy reversal
    Title
    Incidence of severe intestinal dysfunction at 2 years after ostomy reversal
    Description
    Incidence of severe intestinal dysfunction at 2 years after ostomy reversal
    Time Frame
    2 years after ostomy reversal
    Title
    Incidence of severe intestinal dysfunction at 3 years after ostomy reversal
    Description
    Incidence of severe intestinal dysfunction at 3 years after ostomy reversal
    Time Frame
    3 years after ostomy reversal
    Title
    Quality of life at 1 year after ostomy reversal
    Description
    Quality of life at 1 year after ostomy reversal
    Time Frame
    1 year after ostomy reversal
    Title
    Quality of life at 2 years after ostomy reversal
    Description
    Quality of life at 2 years after ostomy reversal
    Time Frame
    2 years after ostomy reversal
    Title
    Quality of life at 3 years after ostomy reversal
    Description
    Quality of life at 3 years after ostomy reversal
    Time Frame
    3 years after ostomy reversal

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    70 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: 1. Patients aged 18-70 years; 2. Patients with Eastern Cooperative Oncology Group (ECOG) physical condition score of 0-2; 3. Patients with previous pathological diagnosis of pelvic tumors (Gynecology, prostate, urinary system); 4. Patients with a history of pelvic radiotherapy, at least 6 months from the end of the last radiotherapy; 5. Patients without recurrence or metastasis of primary tumor; 6. The late complications of CRII patients, such as deep rectal ulcer (VRS score >=3), rectal sigmoid colon stenosis, obstruction, chronic perforation, rectal necrosis, rectovaginal fistula, intractable anal pain caused by rectal lesions, intractable rectal bleeding which is still difficult to be relieved by stoma operation, and patients who need sigmoid colorectal resection; 7. Patients who can tolerate general anesthesia; 8. The subjects and their families are able to understand the study plan, willing to participate and sign the informed consent. Exclusion Criteria: 1. Patients with acute intestinal obstruction, acute intestinal perforation and intestinal hemorrhage who need emergency operation; 2. Patients with severe pelvic adhesion and frozen pelvis; 3. Patients with unstable primary tumor or tumor in other parts; 4. Patients who need to undergo combined organ resection; 5. Patients with a history of sigmoidostomy; 6. American society of anesthesiologists (ASA) level IV to V; 7. Patients with serious mental illness; 8. Pregnant or lactating women; 9. Patients with serious cardiovascular disease, uncontrollable infection, or other uncontrollable combined diseases.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Tenghui Ma, PhD
    Phone
    13560232462
    Email
    matengh@mail.sysu.edu.cn

    12. IPD Sharing Statement

    Citations:
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    16080176
    Citation
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    Citation
    Andreyev J. Gastrointestinal symptoms after pelvic radiotherapy: a new understanding to improve management of symptomatic patients. Lancet Oncol. 2007 Nov;8(11):1007-17. doi: 10.1016/S1470-2045(07)70341-8.
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    PubMed Identifier
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    Citation
    Perrakis N, Athanassiou E, Vamvakopoulou D, Kyriazi M, Kappos H, Vamvakopoulos NC, Nomikos I. Practical approaches to effective management of intestinal radiation injury: benefit of resectional surgery. World J Gastroenterol. 2011 Sep 21;17(35):4013-6. doi: 10.3748/wjg.v17.i35.4013.
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    PubMed Identifier
    28153025
    Citation
    Zhong Q, Yuan Z, Ma T, Wang H, Qin Q, Chu L, Wang J, Wang L. Restorative resection of radiation rectovaginal fistula can better relieve anorectal symptoms than colostomy only. World J Surg Oncol. 2017 Feb 2;15(1):37. doi: 10.1186/s12957-017-1100-0.
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    PubMed Identifier
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    Citation
    Meissner K. Late radiogenic small bowel damage: guidelines for the general surgeon. Dig Surg. 1999;16(3):169-74. doi: 10.1159/000018721.
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    PubMed Identifier
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    Citation
    Qin Q, Zhu Y, Wu P, Fan X, Huang Y, Huang B, Wang J, Wang L. Radiation-induced injury on surgical margins: a clue to anastomotic leakage after rectal-cancer resection with neoadjuvant chemoradiotherapy? Gastroenterol Rep (Oxf). 2019 Apr;7(2):98-106. doi: 10.1093/gastro/goy042. Epub 2018 Dec 11.
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    PubMed Identifier
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    Citation
    He Y, Zhou Z, Huang X, Guan Q, Qin Q, Zhu M, Wang H, Zhong Q, Chen D, Wang H, Fang L, Ma T. Laparoscopic Proximally Extended Colorectal Resection With Two-Stage Turnbull-Cutait Pull-Through Coloanal Anastomosis for Late Complications of Chronic Radiation Proctopathy. Front Surg. 2022 Apr 25;9:845148. doi: 10.3389/fsurg.2022.845148. eCollection 2022.
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    PE-Bacon for Late Complications of Chronic Radiation-induced Rectal Injury

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