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Active Surgical Intervention on Crohn's Disease

Primary Purpose

Crohn Disease

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
active surgical intervention
Sponsored by
Wuxi People's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohn Disease

Eligibility Criteria

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

Inclusion Criteria:

  1. Moderate to severe active CD (CDAI ≥ 150)
  2. Endoscopic subscore meet the criteria (SES-CD ≥ 4)
  3. Patients aged 18 to 75 years with established diagnosis of CD

Exclusion Criteria:

  1. Mild active CD (CDAI < 150)
  2. More than 25mg of prednisolone per day (or equivalent steroid)
  3. Previous colonic surgery
  4. Active gastrointestinal infection
  5. Pregnancy
  6. Anticoagulant therapy or duel antiplatelet therapy (i.e. aspirin and clopidogrel)
  7. Current use of antibiotics
  8. Anti-TNF therapy

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Other

    Arm Label

    active enterostomy

    Arm Description

    active enterostomy before serious complications

    Outcomes

    Primary Outcome Measures

    SES-CD
    Simple Endoscopic Score for Crohn's Disease

    Secondary Outcome Measures

    CDAI
    Crohn's Disease Activity Index

    Full Information

    First Posted
    August 25, 2022
    Last Updated
    August 28, 2022
    Sponsor
    Wuxi People's Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05523050
    Brief Title
    Active Surgical Intervention on Crohn's Disease
    Official Title
    Effect of Active Surgical Intervention on Disease Remission in Patients With Crohn's Disease: A Single-Arm Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 16, 2022 (Anticipated)
    Primary Completion Date
    March 16, 2024 (Anticipated)
    Study Completion Date
    May 16, 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Wuxi 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
    The study is to determine whether active surgical intervention promotes disease remission in patients with Crohn's Disease (CD).The management of CD involves both maintenance medication and medication used to control flares of the disease. The goal of maintenance therapy in CD is to maintain steroid- free remission, clinically and endoscopically. This requires regular clinical assessment including history, physical examination and at times colonoscopic examination. Other tools of assessment include blood (e.g. CRP, WCC) and stool (calprotectin) testing for inflammatory markers and imaging including MRI, CT or ultrasound. The choice of maintenance treatment in CD is determined by disease extent, disease course (frequency of flares), failure of previous maintenance treatment, severity of the most recent flare, treatment used for inducing remission during the most recent flare, safety of maintenance treatment, and cancer prevention. The mainstay of maintenance medication are the 5-aminosalicylic acid compounds (5-ASA) such as mesalazine or sulphasalazine. These compounds are commonly taken orally in formulations that predominantly deliver the active 5-ASA component to the colon. Alternatively, or in addition, mesalazine preparations can be delivered topically via enema or suppository if the disease only involves the left side of the colon (although it is only PBS funded for topical therapy during a flare and not for maintenance of remission - even though it also works in this setting). The majority of patients can be managed with maintenance 5-ASA compounds most of the time. For patients who have repeated flares of disease on 5-ASA maintenance therapy (1 or more flares in a year needing steroids), thiopurine medication such as azathioprine or 6-mercapropurine should be used. These medications induce systemic immunosuppression, reduce the incidence and severity of flares of colitis but also slightly increase the risk of some infections and malignancy. Anti TNF agents such as infliximab or adalimumab have been shown to have benefit in maintaining remission in CD (and are licensed for this indication by the TGA), however these agents are very expensive and not funded by the pharmaceutical benefits scheme in Australia and so, are not readily available. The anti TNF agents also give an increased risk of infection, particularly latent TB reactivation. Mild flares of CD can be managed with higher doses of oral 5-ASA compounds or the addition of topical 5-ASAs given via enema or suppository. More severe flares are usually managed with a course of systemic corticosteroid. These can be given intravenously in acute, severe disease or orally in less severe flares. The steroids should then be tapered over time and discontinued. There is no indication for long term steroid use in CD and prolonged steroid use is associated with a number of complications including infection, osteoporosis, obesity, diabetes, poor wound healing, thinning skin, mood changes and insomnia. Severe flares of CD not responsive to steroids may respond to rescue therapy with the addition of either cyclosporin or anti-TNF therapy. Patients in whom colonic inflammation cannot be controlled adequately frequently undergo total colectomy. This may be done electively (for refractory disease) or emergently in acute fulminant colitis. Colectomy entails surgical risk that is higher in the emergent setting; this risk includes infection, wound breakdown and a mortality rate. Colectomy is considered "curative" for CD especially if they have an ileostomy stoma created, however, it frequently also leads to complications both short- and long-term. In addition, in patients in whom an ileal-anal pouch is fashioned up to 50% will subsequently develop pouchitis at 4 years post surgery. Patient eligibility was determined during a 5-week screening period, during which time details on patient demographics, medical history, and previous and concomitant medications were obtained,and the following assessments were completed: viral serology, stool culture, Crohn's Disease Activity Index (CDAI) patient diary and clinical score, Simple Endoscopic Score for Crohn's Disease (SES-CD), colonoscopy and colonic biopsy, stool collection for faecal biomarkers, vital signs, and laboratory evaluations. All participants need to be subjected to rigorous assessments mentioned above at week 4, week 8 and week 12 after receiving active surgical intervention (two kinds: one is colostomy, and the other one is colonic exclusion).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Crohn Disease

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    100 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    active enterostomy
    Arm Type
    Other
    Arm Description
    active enterostomy before serious complications
    Intervention Type
    Procedure
    Intervention Name(s)
    active surgical intervention
    Intervention Description
    two kinds: one is colostomy, and the other one is colonic exclusion
    Primary Outcome Measure Information:
    Title
    SES-CD
    Description
    Simple Endoscopic Score for Crohn's Disease
    Time Frame
    12 weeks
    Secondary Outcome Measure Information:
    Title
    CDAI
    Description
    Crohn's Disease Activity Index
    Time Frame
    12 weeks

    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: Moderate to severe active CD (CDAI ≥ 150) Endoscopic subscore meet the criteria (SES-CD ≥ 4) Patients aged 18 to 75 years with established diagnosis of CD Exclusion Criteria: Mild active CD (CDAI < 150) More than 25mg of prednisolone per day (or equivalent steroid) Previous colonic surgery Active gastrointestinal infection Pregnancy Anticoagulant therapy or duel antiplatelet therapy (i.e. aspirin and clopidogrel) Current use of antibiotics Anti-TNF therapy
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Wei Shen, PhD, MD
    Phone
    +86 133 5811 0723
    Email
    shenweijs@outlook.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Peihua Lu, PhD, MD
    Organizational Affiliation
    The Affiliated Wuxi People's Hospital of Nanjing Medical University
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    To determine whether active surgical intervention promotes disease remission in patients with Crohn's Disease (CD).

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