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Early Surgery Versus Conservative Treatment in Patients With Ileocaecal Crohn's Disease (ESPRIT)

Primary Purpose

Crohn's Disease

Status
Unknown status
Phase
Not Applicable
Locations
Czech Republic
Study Type
Interventional
Intervention
Ileocaecal resection
Sponsored by
Ondrej Ryska
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohn's Disease focused on measuring Early surgery, Crohn's disease, Step-up therapy

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria

  • All patients aged 18-65 years with a uncomplicated ileocaecal form of Crohn's disease (affected < 20 cm of terminal ileum) (type: L1B1) diagnosed within last 12 months
  • Diagnose confirmed by endoscopy including appropriate extent of disease and presence of ulcers in terminal ileum
  • Patient is able to understand the study and sign an informed consent

Exclusion Criteria:

  • Pregnant or breastfeeding women
  • Previous bowel resection or other extensive abdominal surgery, which primarily excludes laparoscopic approach
  • Affected other parts of the digestive tract or symptomatic stenosis or stenosis impassable for the endoscope or presence of prestenotic dilatation in terminal ileum confirmed by enterography
  • Any extraluminal complications of Crohn's disease (fistula, abscess)
  • Affected part of terminal ileum longer than 20 cm
  • Severe comorbidities (heart failure, renal failure, liver failure, severe disorders of the central and peripheral nervous system, serious infectious disease) or patient with ASA (American Society of Anesthesiologists) III and more
  • Malnutrition or presence of another serious risk factor, which contradicts construction of primary anastomosis
  • Current use of immunosuppressive or biologic therapy

Other exclusion criteria:

  • Different intraoperative finding
  • Protocol violation
  • Subject refuses further participation in the study
  • Termination of the trial by responsible authority

Sites / Locations

  • The University Hospital Brno
  • Hospital Ceske Budejovice
  • Horovice Hospital
  • Universitiy Hospital Hradec Kralove
  • Hospital Jihlava
  • Hospital Liberec
  • Vitkovice Hospital
  • University Hospital in Pilsen
  • Royal Vinohrady University Hospital
  • Institute for Clinical and Experimental Medicine
  • Na Homolce Hospital
  • ISCARE

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Early Surgery - ES

Step-up therapy - STUP

Arm Description

Early laparoscopic ileocaecal resection

Treatment with step-up conservative approach according to good clinical practice.

Outcomes

Primary Outcome Measures

Endoscopic remission
The rate of endoscopic remission defined as Rutgeerts score ≤ 1 and SES-CD = 0 in early surgery and standard step-up therapy group respectively

Secondary Outcome Measures

QoL
Quality of life measured by IBDQ, IBD Disability index
Clinical remission
Clinical remission defined by Crohn's disease activity index < 150
Drug consumption
Overall drug consumption (corticosteroids, antibiotics, immunomodulators, biologic therapy)

Full Information

First Posted
March 17, 2016
Last Updated
April 26, 2016
Sponsor
Ondrej Ryska
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1. Study Identification

Unique Protocol Identification Number
NCT02716454
Brief Title
Early Surgery Versus Conservative Treatment in Patients With Ileocaecal Crohn's Disease
Acronym
ESPRIT
Official Title
Early Surgery Versus Conservative Treatment in Patients With Ileocaecal Crohn's Disease - Prospective Randomized Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2016
Overall Recruitment Status
Unknown status
Study Start Date
May 2016 (undefined)
Primary Completion Date
May 2021 (Anticipated)
Study Completion Date
December 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Ondrej Ryska

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study compares the efficacy of early surgical with medical treatment in patients with ileocaecal uncomplicated Crohn's disease. The patients with affected short part of terminal ileum will be randomized either for laparoscopic ileocaecal resection or standard step-up pharmacological therapy.
Detailed Description
Surgical therapy is currently indicated for Crohn's disease (CD) patients after conservative treatment becomes ineffective. The principles of so-called step-up therapy (STUP) where surgery represents the last therapeutical option are still followed. Early surgical intervention (Early Surgery - ES) can be an alternative even in patients with uncomplicated type of CD before all medical therapy is used (Top-down approach). Limited resection under these conditions will lead to immediate remission. Moreover, laparoscopic ileocaecal resection is safe with low morbidity and regarding potential complications of step-up treatment might be beneficial for the patient. Before wide introduction of ES approach into clinical practice, it is necessary to perform a randomized trial comparing early resection with the standard step-up medical therapy. The potential effect of early, intensive therapy (ileocaecal resection) on biological behavior of the disease has not been studied that is why patients with uncomplicated ileocaecal form are the most suitable for such a trial. Significant number of these patients will indeed progress into more unfavorable course of the disease (relapse, complicated form, early recurrence). Other potential benefit of early resection is the extended period without necessary medication. Even pharmacological recurrence prevention is not needed after surgery in uncomplicated CD patient if other risk factors are excluded. Rapid remission induced by surgery can lead to faster improvement of quality of life than long-term medication.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn's Disease
Keywords
Early surgery, Crohn's disease, Step-up therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Early Surgery - ES
Arm Type
Experimental
Arm Description
Early laparoscopic ileocaecal resection
Arm Title
Step-up therapy - STUP
Arm Type
No Intervention
Arm Description
Treatment with step-up conservative approach according to good clinical practice.
Intervention Type
Procedure
Intervention Name(s)
Ileocaecal resection
Intervention Description
laparoscopic ileocaecal resection with primary anastomosis
Primary Outcome Measure Information:
Title
Endoscopic remission
Description
The rate of endoscopic remission defined as Rutgeerts score ≤ 1 and SES-CD = 0 in early surgery and standard step-up therapy group respectively
Time Frame
24 months
Secondary Outcome Measure Information:
Title
QoL
Description
Quality of life measured by IBDQ, IBD Disability index
Time Frame
24 months
Title
Clinical remission
Description
Clinical remission defined by Crohn's disease activity index < 150
Time Frame
24 months
Title
Drug consumption
Description
Overall drug consumption (corticosteroids, antibiotics, immunomodulators, biologic therapy)
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria All patients aged 18-65 years with a uncomplicated ileocaecal form of Crohn's disease (affected < 20 cm of terminal ileum) (type: L1B1) diagnosed within last 12 months Diagnose confirmed by endoscopy including appropriate extent of disease and presence of ulcers in terminal ileum Patient is able to understand the study and sign an informed consent Exclusion Criteria: Pregnant or breastfeeding women Previous bowel resection or other extensive abdominal surgery, which primarily excludes laparoscopic approach Affected other parts of the digestive tract or symptomatic stenosis or stenosis impassable for the endoscope or presence of prestenotic dilatation in terminal ileum confirmed by enterography Any extraluminal complications of Crohn's disease (fistula, abscess) Affected part of terminal ileum longer than 20 cm Severe comorbidities (heart failure, renal failure, liver failure, severe disorders of the central and peripheral nervous system, serious infectious disease) or patient with ASA (American Society of Anesthesiologists) III and more Malnutrition or presence of another serious risk factor, which contradicts construction of primary anastomosis Current use of immunosuppressive or biologic therapy Other exclusion criteria: Different intraoperative finding Protocol violation Subject refuses further participation in the study Termination of the trial by responsible authority
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ondrej Ryska, Dr, PhD
Phone
606254686
Ext
00420
Email
ondrejryska@centrum.cz
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ondrej Ryska, Dr, PhD
Organizational Affiliation
Section of IBD surgery - Czech Surgical Society
Official's Role
Principal Investigator
Facility Information:
Facility Name
The University Hospital Brno
City
Brno
ZIP/Postal Code
625 00
Country
Czech Republic
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lenka Prokopova, Dr.
Email
lprokopova@fnbrno.cz
First Name & Middle Initial & Last Name & Degree
Filip Marek, Dr.
Email
fmarek@fnbrno.cz
Facility Name
Hospital Ceske Budejovice
City
Ceske Budejovice
ZIP/Postal Code
370 01
Country
Czech Republic
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Olga Shonova, Dr.
Email
shonova@nemcb.cz
First Name & Middle Initial & Last Name & Degree
M Kobza, Dr.
Email
mkobza@seznam.cz
Facility Name
Horovice Hospital
City
Horovice
ZIP/Postal Code
26831
Country
Czech Republic
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zuzana Serclova, Dr
Email
sercl@seznam.cz
Facility Name
Universitiy Hospital Hradec Kralove
City
Hradec Kralove
ZIP/Postal Code
50005
Country
Czech Republic
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Julius Orhalmi, Dr.
Email
orhalmi@volny.cz
Facility Name
Hospital Jihlava
City
Jihlava
ZIP/Postal Code
586 33
Country
Czech Republic
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marie Tomanova, Dr.
Email
tomanovam@nemji.cz
Facility Name
Hospital Liberec
City
Liberec
ZIP/Postal Code
460 63
Country
Czech Republic
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lenka Nedbalova, Dr.
Email
lenka.nedbalova@nemlib.cz
Facility Name
Vitkovice Hospital
City
Ostrava - Vitkovice
ZIP/Postal Code
703 84
Country
Czech Republic
Facility Name
University Hospital in Pilsen
City
Pilsen
ZIP/Postal Code
323 18
Country
Czech Republic
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jana Kozeluhova, Dr.
Email
kozeluhova@fnplzen.cz
Facility Name
Royal Vinohrady University Hospital
City
Prague
ZIP/Postal Code
100 34
Country
Czech Republic
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pavel Lisý, Dr.
Email
lisy@fnkv.cz
Facility Name
Institute for Clinical and Experimental Medicine
City
Prague
ZIP/Postal Code
140 21
Country
Czech Republic
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pavel Drastich, Dr.
Email
drastich@hotmail.com
Facility Name
Na Homolce Hospital
City
Prague
ZIP/Postal Code
150 00
Country
Czech Republic
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Karel Mareš, Dr
Email
karel.mares@homolka.cz
Facility Name
ISCARE
City
Prague
ZIP/Postal Code
170 00
Country
Czech Republic
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dana Duricova, Dr
Email
dana.duricova@seznam.cz

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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Early Surgery Versus Conservative Treatment in Patients With Ileocaecal Crohn's Disease

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