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Simplified Bowel Preparation Versus Standard Bowel Preparation Before Capsule Endoscopy in Patients With Crohn's Disease (CROHN-PREP)

Primary Purpose

Crohn Disease

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
capsule endoscopy
standard small bowel preparation
Simplified small bowel preparation
Sponsored by
Nantes University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Crohn Disease

Eligibility Criteria

15 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients of both genders aged over 18 years old
  • With an established diagnosis of Crohn's disease, whether active or quiescent
  • With an indication of a small bowel capsule endoscopy
  • Without any small bowel stricture (patency capsule procedure on the 7 days before the capsule endoscopy)
  • Registered with a social security scheme
  • Having provided their oral consent for the study after appropriate information

Exclusion Criteria:

  • - Patients aged below 18 years old
  • Diagnosis of ulcerative colitis or IBD unclassified
  • Presence of an ileostomy
  • Presence of a small bowel syndrome
  • Symptoms suggestive of a small bowel stricture
  • Retention of the patency capsule on an abdominal X-ray performed 48 hours after the ingestion
  • Abdominal pain after the ingestion of the patency capsule
  • Planned abdominal surgery in the next month
  • Known intestinal fistula
  • Swallowing disorders
  • Established diagnosis of delayed gastric emptying or suggestive symptoms
  • Intake of non-steroidal anti-inflammatory drugs (NSAIDs) in the month prior to the capsule endoscopy
  • Intake of oral iron supplementation in the week prior to the capsule endoscopy
  • Intake of oral 5-ASA granules in the week prior to the capsule endoscopy
  • Ongoing pregnancy
  • Presence of a pace-maker or implantable defibrillator
  • Known allergy to polyethylene glycol or to lactose
  • Vulnerable people i.e. adults under a legal protection regime (guardianship, trusteeship, judicial safeguard)

Sites / Locations

  • Angers University Hospital
  • Brest University hospital
  • Cholet hospital
  • Vendée departmental hospital
  • Clinique Jules Verne
  • Hopital privé Confluent
  • Nantes University HospitalRecruiting
  • Rennes University hospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard small bowel preparation

Simplified small bowel preparation

Arm Description

2 L of polyethylene glycol and free residue diet the day before the capsule endoscopy. 2 mL of Babyspasmyl after ingestion of capsule

Liquid diet the evening before and water on the morning of the capsule endoscopy. 2 mL of Babyspasmyl after ingestion of capsule

Outcomes

Primary Outcome Measures

KODA score (entire small bowel)
Small bowel preparation quality (entire small bowel)

Secondary Outcome Measures

KODA score for each small bowel segment
Small bowel preparation quality (by segment : upper/middle/lower third)
Qualitative assessment by the reader
Proportion of images in which preparation is considered as "good", "moderate" or "low" by the reader (by segment)
Quantitative assessment of acceptability of preparation
Patient's acceptability of the bowel preparation on a visual analog scale between 0 (nil) to 10 (excellent)
Quantitative assessment on a visual analog scale between 0 (nil) to 10 (excellent)
Patient's acceptability of the examination on a visual analog scale between 0 (nil) to 10 (excellent)
Lewis score
Diagnostic yield evaluation
complete examinations
Percentage of complete examinations defined by the visualization of the first duodenal image and the first caecal image
Small bowel transit time
Recording time between the visualization of the first duodenal image and the first caecal image, if visualized

Full Information

First Posted
October 21, 2021
Last Updated
December 19, 2022
Sponsor
Nantes University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05117996
Brief Title
Simplified Bowel Preparation Versus Standard Bowel Preparation Before Capsule Endoscopy in Patients With Crohn's Disease
Acronym
CROHN-PREP
Official Title
Simplified Bowel Preparation Versus Standard Bowel Preparation Before Capsule Endoscopy in Patients With Crohn's Disease: a Prospective Randomized Controlled Multicenter Study
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 5, 2022 (Actual)
Primary Completion Date
July 2024 (Anticipated)
Study Completion Date
July 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nantes University Hospital

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
The European guidelines currently recommend to use 2 L of polyethylene glycol and free residue diet before any capsule endoscopy. However, up to now, no studies have been conducted to specifically evaluate bowel preparation modalities before small bowel capsule endoscopy in patients with Crohn's disease. In patients with Crohn's disease and small bowel ulcers, polyethylene glycol may remove some fibrin from these ulcers and alter bowel preparation. Moreover, it is important to select the most acceptable bowel preparation because patients with Crohn's disease will have to repeat capsule endoscopy several times after initiating treatment, for monitoring under treatment, or for detection of post-operative recurrence. In a preliminary retrospective study, it has been suggested that a simplified bowel preparation with liquid diet the evening before and water on the morning of the capsule endoscopy induced a better bowel preparation than the standard method with polyethylene glycol. Thus, the aim of the study is to demonstrate the superiority of this simplified bowel preparation compared to the standard preparation modality in terms of quality of bowel preparation, patient's acceptability and diagnostic yield.
Detailed Description
Crohn's disease is a chronic inflammatory bowel disease characterized by the presence of ulcers that can affect the entire digestive tract, from the mouth to the anus. The existence of small bowel lesions is pejorative and associated with poorer outcomes and a higher risk of intestinal resection. Small bowel capsule endoscopy allows the visualization of the entire small bowel in a non-invasive and outpatient setting, without any anesthesia. It is the exam with the best diagnostic yield for the detection of small bowel ulcers in patients with Crohn's disease. Moreover, it allows the monitoring of patients after initiating treatment to assess mucosal healing and the detection of post-operative recurrence. As for any endoscopic examinations, its acceptability depends on bowel preparation modalities. The European Society of Gastrointestinal Endoscopy (ESGE) currently recommends to use 2 L of polyethylene glycol and free residue diet before any capsule endoscopy. However, patients with Crohn's disease were a minority (< 1.5 %) in the studies on which these guidelines are based on. Yet, in patients with small bowel Crohn's disease, polyethylene glycol may remove some fibrin from the ulcers and hence, alter bowel preparation. Moreover, it is important to select the most acceptable bowel preparation because patients with Crohn's disease will have to repeat capsule endoscopy several times after initiating treatment, for monitoring under treatment, or for detection of post-operative recurrence. A preliminary retrospective study suggested that a simplified bowel preparation with liquid diet the evening before and water on the morning of the capsule endoscopy induced a better bowel preparation than the standard method with polyethylene glycol. Thus, the aim of CROHN-PREP study is to demonstrate the superiority of this simplified bowel preparation compared to the standard preparation modality in terms of quality of bowel preparation, patient's acceptability and diagnostic yield.

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
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Masking Description
Single blind
Allocation
Randomized
Enrollment
144 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard small bowel preparation
Arm Type
Active Comparator
Arm Description
2 L of polyethylene glycol and free residue diet the day before the capsule endoscopy. 2 mL of Babyspasmyl after ingestion of capsule
Arm Title
Simplified small bowel preparation
Arm Type
Experimental
Arm Description
Liquid diet the evening before and water on the morning of the capsule endoscopy. 2 mL of Babyspasmyl after ingestion of capsule
Intervention Type
Other
Intervention Name(s)
capsule endoscopy
Intervention Description
capsule endoscopy
Intervention Type
Other
Intervention Name(s)
standard small bowel preparation
Intervention Description
2 L of polyethylene glycol and free residue diet the day before the capsule endoscopy. 2 mL of Babyspasmyl after ingestion of capsule
Intervention Type
Other
Intervention Name(s)
Simplified small bowel preparation
Intervention Description
Liquid diet the evening before and water on the morning of the capsule endoscopy. 2 mL of Babyspasmyl after ingestion of capsule
Primary Outcome Measure Information:
Title
KODA score (entire small bowel)
Description
Small bowel preparation quality (entire small bowel)
Time Frame
through the reading of the capsule endoscopy, an average of 6 months
Secondary Outcome Measure Information:
Title
KODA score for each small bowel segment
Description
Small bowel preparation quality (by segment : upper/middle/lower third)
Time Frame
through the reading of the capsule endoscopy, an average of 6 months
Title
Qualitative assessment by the reader
Description
Proportion of images in which preparation is considered as "good", "moderate" or "low" by the reader (by segment)
Time Frame
through the reading of the capsule endoscopy, an average of 6 months
Title
Quantitative assessment of acceptability of preparation
Description
Patient's acceptability of the bowel preparation on a visual analog scale between 0 (nil) to 10 (excellent)
Time Frame
Immediately before the capsule endoscopy
Title
Quantitative assessment on a visual analog scale between 0 (nil) to 10 (excellent)
Description
Patient's acceptability of the examination on a visual analog scale between 0 (nil) to 10 (excellent)
Time Frame
Immediately before the capsule endoscopy
Title
Lewis score
Description
Diagnostic yield evaluation
Time Frame
through the reading of the capsule endoscopy, an average of 6 months
Title
complete examinations
Description
Percentage of complete examinations defined by the visualization of the first duodenal image and the first caecal image
Time Frame
through the reading of the capsule endoscopy, an average of 6 months
Title
Small bowel transit time
Description
Recording time between the visualization of the first duodenal image and the first caecal image, if visualized
Time Frame
through the reading of the capsule endoscopy, an average of 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients of both genders aged over 18 years old With an established diagnosis of Crohn's disease, whether active or quiescent With an indication of a small bowel capsule endoscopy Without any small bowel stricture (patency capsule procedure on the 7 days before the capsule endoscopy) Registered with a social security scheme Having provided their oral consent for the study after appropriate information Exclusion Criteria: - Patients aged below 18 years old Diagnosis of ulcerative colitis or IBD unclassified Presence of an ileostomy Presence of a small bowel syndrome Symptoms suggestive of a small bowel stricture Retention of the patency capsule on an abdominal X-ray performed 48 hours after the ingestion Abdominal pain after the ingestion of the patency capsule Planned abdominal surgery in the next month Known intestinal fistula Swallowing disorders Established diagnosis of delayed gastric emptying or suggestive symptoms Intake of non-steroidal anti-inflammatory drugs (NSAIDs) in the month prior to the capsule endoscopy Intake of oral iron supplementation in the week prior to the capsule endoscopy Intake of oral 5-ASA granules in the week prior to the capsule endoscopy Ongoing pregnancy Presence of a pace-maker or implantable defibrillator Known allergy to polyethylene glycol or to lactose Vulnerable people i.e. adults under a legal protection regime (guardianship, trusteeship, judicial safeguard)
Facility Information:
Facility Name
Angers University Hospital
City
Angers
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nina DIB
Facility Name
Brest University hospital
City
Brest
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Franck CHOLET
Facility Name
Cholet hospital
City
Cholet
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mehdi Kaasis
Facility Name
Vendée departmental hospital
City
La Roche-sur-Yon
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Astrid DE MAISSIN
Facility Name
Clinique Jules Verne
City
Nantes
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mathurin Flamant
Email
mathurinflamant@hotmail.com
First Name & Middle Initial & Last Name & Degree
Mathurin Flamant
Facility Name
Hopital privé Confluent
City
Nantes
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Caroline Trang
Email
dr.trangpoisson@groupeconfluent.fr
First Name & Middle Initial & Last Name & Degree
Caroline Trang
Facility Name
Nantes University Hospital
City
Nantes
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Catherine LE BERRE
Phone
+332 44 768391
Email
catherine.leberre@chu-nantes.fr
First Name & Middle Initial & Last Name & Degree
Catherine LE BERRE
Facility Name
Rennes University hospital
City
Rennes
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Guillaume BOUGUEN
Phone
0299289889
Email
guillaume.bouguen@chu-rennes.fr
First Name & Middle Initial & Last Name & Degree
Guillaume BOUGUEN

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Simplified Bowel Preparation Versus Standard Bowel Preparation Before Capsule Endoscopy in Patients With Crohn's Disease

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