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
About this trial
This is an interventional treatment trial for Crohn Disease
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
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
NCT ID
NCT05523050
First Posted
August 25, 2022
Last Updated
August 28, 2022
Sponsor
Wuxi People's Hospital
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).
Learn more about this trial
Active Surgical Intervention on Crohn's Disease
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