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KONO-S Anastomosis Compared to Conventional Ileocolonic Anastomosis to Reduce Recurrence in Crohn's Disease (KOALA)

Primary Purpose

Crohn Disease

Status
Not yet recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Kono-S anastomosis
Conventional anastomosis for ileocolonicresection of Crohn's disease
Sponsored by
Centre Hospitalier Universitaire de Besancon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohn Disease focused on measuring Crohn's disease, Kono-S anastomosis, conventional anastomosis, endoscopic recurrence

Eligibility Criteria

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

Inclusion Criteria: Adult patient ≥ 18 years and ≤75 years With Crohn's disease. Requiring a first ileocolonic resection: fistulizing, abscessed, or stenosing disease or disease refractory to medical treatment. Affiliated to the French social security system. Exclusion Criteria: Previous ileocolonic resection Contraindication to postoperative endoscopy. Anastomosis with a planned defunctioning protective stoma. Emergency surgery (peritonitis). Lack of consent to the study. Pregnant patients. Refusal to participate or inability to provide informed consent. Patient under legal protection (individuals under guardianship by court order)

Sites / Locations

  • CHu de Besançon

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Kono-S group

Control group

Arm Description

Kono-S group, in which ileocolonic anastomosis will be performed following the technique described by Kono et al.

Conventional side-to-side ileocolonic anastomosis

Outcomes

Primary Outcome Measures

endoscopy score
Rutgeerts endoscopy score ≥ i2 (>5 anastomotic lesions with passable stenosis (skip lesions); or lesions in the area of the anastomosis) at 6 months obtained by centralized double reading of filmed endoscopy. I0 no lesions 1 <5 aphthous lesions in the neoterminal ileum 2 >5 anastomotic lesions with passable stenosis (skip lesions); or lesions in the area of the anastomosis 3 diffuse ileitis 4 diffuse ileitis with deep ulcerations and/or Stenosis

Secondary Outcome Measures

Harvey-Bradshaw Index (HBI)
Harvey-Bradshaw Index (HBI) Disease not active: <4 ; Mild disease activity: HBI >= 4 and <= 8 ; Moderate disease activity: HBI > 8 and <= 12 ; Severe disease activity: HBI > 12
Harvey-Bradshaw Index (HBI)
Harvey-Bradshaw Index (HBI) Disease not active: <4 ; Mild disease activity: HBI >= 4 and <= 8 ; Moderate disease activity: HBI > 8 and <= 12 ; Severe disease activity: HBI > 12
Harvey-Bradshaw Index (HBI)
Harvey-Bradshaw Index (HBI) Disease not active: <4 ; Mild disease activity: HBI >= 4 and <= 8 ; Moderate disease activity: HBI > 8 and <= 12 ; Severe disease activity: HBI > 12
Harvey-Bradshaw Index (HBI)
Harvey-Bradshaw Index (HBI) Disease not active: <4 ; Mild disease activity: HBI >= 4 and <= 8 ; Moderate disease activity: HBI > 8 and <= 12 ; Severe disease activity: HBI > 12
Crohn's Disease Activity Index (CDAI) clinical scores
Crohn's Disease Activity Index (CDAI) clinical scores The patients with CD can be divided into asymptomatic remission (CDAI < 150), mild-to-moderate CD (150-220), moderate-to-severe CD (220-450), and severe-fulminant disease (>450).
Crohn's Disease Activity Index (CDAI) clinical scores
Crohn's Disease Activity Index (CDAI) clinical scores The patients with CD can be divided into asymptomatic remission (CDAI < 150), mild-to-moderate CD (150-220), moderate-to-severe CD (220-450), and severe-fulminant disease (>450).
Crohn's Disease Activity Index (CDAI) clinical scores
Crohn's Disease Activity Index (CDAI) clinical scores The patients with CD can be divided into asymptomatic remission (CDAI < 150), mild-to-moderate CD (150-220), moderate-to-severe CD (220-450), and severe-fulminant disease (>450).
Crohn's Disease Activity Index (CDAI) clinical scores
Crohn's Disease Activity Index (CDAI) clinical scores The patients with CD can be divided into asymptomatic remission (CDAI < 150), mild-to-moderate CD (150-220), moderate-to-severe CD (220-450), and severe-fulminant disease (>450).
Fecal calprotectin
Fecal calprotectin
Fecal calprotectin
Fecal calprotectin

Full Information

First Posted
July 26, 2023
Last Updated
August 21, 2023
Sponsor
Centre Hospitalier Universitaire de Besancon
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1. Study Identification

Unique Protocol Identification Number
NCT05974358
Brief Title
KONO-S Anastomosis Compared to Conventional Ileocolonic Anastomosis to Reduce Recurrence in Crohn's Disease
Acronym
KOALA
Official Title
KONO-S Anastomosis Compared to Conventional Ileocolonic Anastomosis to Reduce Recurrence in Crohn's Disease: a Superiority Phase III Prospective, Randomized, Multicenter, Double-blind Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 1, 2024 (Anticipated)
Primary Completion Date
January 31, 2028 (Anticipated)
Study Completion Date
January 31, 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Besancon

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
Crohn's disease (CD) is a chronic inflammatory bowel disease (IBD) currently affecting one person in a thousand in France. It can lead to numerous digestive complications such as fistulas, abscesses or stenosis. Despite numerous therapeutic advances, the rate of patients requiring surgery remains very high, with approximately 50% requiring at least one surgical intervention at 10 years after disease diagnosis. However, surgical treatment is not curative, the postoperative recurrence rate being very high, from 65 to-90% endoscopic recurrence at 1 year. The ileocolonic anastomosis is the main site of postoperative recurrence currently defined by a Rutgeerts score (≥i2) 6 months after surgery. In 2003, Kono et al. described a new operative technique that could reduce the rate of post-operative recurrence: a termino-terminal ileocolonic anastomosis, anti-mesenteric, with a supporting column to prevent distortion and anastomotic stenosis (Kono-S anastomosis). The study showed no decrease in endoscopic recurrence rate at 1 year (83% vs 79%), but a significant decrease in surgical recurrence rate at 5 years (15% vs 0%). Recently, a randomized Italian monocenter study showed a significant decrease in endoscopic recurrence rate at 6 and 18 months (22.2% versus 62.8% and 25% versus 67.4%), as well as a decrease in clinical recurrence. The limitations of this study are its monocentric nature and the lack of centralization of the endoscopic analysis to assess the primary endpoint. This surgical technique has been performed in some centers for ileocolonic Crohn's surgery since 2020. Nevertheless, the level of evidence remains too low to establish practice recommendations. The KOALA study will be the first prospective, multicenter, randomized study comparing KONO-S anastomosis and conventional anastomosis for ileocolonicresection of Crohn's disease, with blinded and centralized evaluation of recurrence.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn Disease
Keywords
Crohn's disease, Kono-S anastomosis, conventional anastomosis, endoscopic recurrence

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
prospective, multicenter,randomized study
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
226 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Kono-S group
Arm Type
Experimental
Arm Description
Kono-S group, in which ileocolonic anastomosis will be performed following the technique described by Kono et al.
Arm Title
Control group
Arm Type
Other
Arm Description
Conventional side-to-side ileocolonic anastomosis
Intervention Type
Procedure
Intervention Name(s)
Kono-S anastomosis
Intervention Description
Kono et al. described a new operative technique that could reduce the rate of post-operative recurrence: a termino-terminal ileocolonic anastomosis, anti-mesenteric, with a supporting column to prevent distortion and anastomotic stenosis (Kono-S anastomosis).
Intervention Type
Procedure
Intervention Name(s)
Conventional anastomosis for ileocolonicresection of Crohn's disease
Intervention Description
conventional anastomosis for ileocolonicresection of Crohn's disease
Primary Outcome Measure Information:
Title
endoscopy score
Description
Rutgeerts endoscopy score ≥ i2 (>5 anastomotic lesions with passable stenosis (skip lesions); or lesions in the area of the anastomosis) at 6 months obtained by centralized double reading of filmed endoscopy. I0 no lesions 1 <5 aphthous lesions in the neoterminal ileum 2 >5 anastomotic lesions with passable stenosis (skip lesions); or lesions in the area of the anastomosis 3 diffuse ileitis 4 diffuse ileitis with deep ulcerations and/or Stenosis
Time Frame
Month 6
Secondary Outcome Measure Information:
Title
Harvey-Bradshaw Index (HBI)
Description
Harvey-Bradshaw Index (HBI) Disease not active: <4 ; Mild disease activity: HBI >= 4 and <= 8 ; Moderate disease activity: HBI > 8 and <= 12 ; Severe disease activity: HBI > 12
Time Frame
Month 6
Title
Harvey-Bradshaw Index (HBI)
Description
Harvey-Bradshaw Index (HBI) Disease not active: <4 ; Mild disease activity: HBI >= 4 and <= 8 ; Moderate disease activity: HBI > 8 and <= 12 ; Severe disease activity: HBI > 12
Time Frame
Month 12
Title
Harvey-Bradshaw Index (HBI)
Description
Harvey-Bradshaw Index (HBI) Disease not active: <4 ; Mild disease activity: HBI >= 4 and <= 8 ; Moderate disease activity: HBI > 8 and <= 12 ; Severe disease activity: HBI > 12
Time Frame
Month 18
Title
Harvey-Bradshaw Index (HBI)
Description
Harvey-Bradshaw Index (HBI) Disease not active: <4 ; Mild disease activity: HBI >= 4 and <= 8 ; Moderate disease activity: HBI > 8 and <= 12 ; Severe disease activity: HBI > 12
Time Frame
Month 24
Title
Crohn's Disease Activity Index (CDAI) clinical scores
Description
Crohn's Disease Activity Index (CDAI) clinical scores The patients with CD can be divided into asymptomatic remission (CDAI < 150), mild-to-moderate CD (150-220), moderate-to-severe CD (220-450), and severe-fulminant disease (>450).
Time Frame
Month 6
Title
Crohn's Disease Activity Index (CDAI) clinical scores
Description
Crohn's Disease Activity Index (CDAI) clinical scores The patients with CD can be divided into asymptomatic remission (CDAI < 150), mild-to-moderate CD (150-220), moderate-to-severe CD (220-450), and severe-fulminant disease (>450).
Time Frame
Month12
Title
Crohn's Disease Activity Index (CDAI) clinical scores
Description
Crohn's Disease Activity Index (CDAI) clinical scores The patients with CD can be divided into asymptomatic remission (CDAI < 150), mild-to-moderate CD (150-220), moderate-to-severe CD (220-450), and severe-fulminant disease (>450).
Time Frame
Month18
Title
Crohn's Disease Activity Index (CDAI) clinical scores
Description
Crohn's Disease Activity Index (CDAI) clinical scores The patients with CD can be divided into asymptomatic remission (CDAI < 150), mild-to-moderate CD (150-220), moderate-to-severe CD (220-450), and severe-fulminant disease (>450).
Time Frame
Month24
Title
Fecal calprotectin
Description
Fecal calprotectin
Time Frame
Month 6
Title
Fecal calprotectin
Description
Fecal calprotectin
Time Frame
Month 12

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: Adult patient ≥ 18 years and ≤75 years With Crohn's disease. Requiring a first ileocolonic resection: fistulizing, abscessed, or stenosing disease or disease refractory to medical treatment. Affiliated to the French social security system. Exclusion Criteria: Previous ileocolonic resection Contraindication to postoperative endoscopy. Anastomosis with a planned defunctioning protective stoma. Emergency surgery (peritonitis). Lack of consent to the study. Pregnant patients. Refusal to participate or inability to provide informed consent. Patient under legal protection (individuals under guardianship by court order)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zaher LAKKIS
Phone
+33381218988
Email
zlakkis@chu-besancon.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Astrid POZET
Phone
+33381218988
Email
apozet@chu-besancon.fr
Facility Information:
Facility Name
CHu de Besançon
City
Besançon
ZIP/Postal Code
25030
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zaher LAKKIS
Email
zlakkis@chu-besancon.fr

12. IPD Sharing Statement

Learn more about this trial

KONO-S Anastomosis Compared to Conventional Ileocolonic Anastomosis to Reduce Recurrence in Crohn's Disease

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