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"Functional Bowel Disorder. Investigation in General Practice"

Primary Purpose

Irritable Bowel Syndrome

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Clinical diagnosis based on symptom criteria
Diagnosis of exclusion
Sponsored by
University of Southern Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Irritable Bowel Syndrome focused on measuring IBS, Irritable bowel syndrome, diagnosis, safety, Health related quality of life

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Fulfill ROME III criteria
  • age 18-50 years
  • signed informed content

Exclusion Criteria:

  • Danger signals (fever, anaemia, weightloss, blod in stools, predisposition for CRC or IBD)
  • abnormal physical examination
  • comorbidity
  • abuse
  • lacking ability to talk and understand danish
  • pregnancy
  • Performed endoscopy within the last 3 years
  • For patients > 40 years. Changed bowel habits, with duration > 3 weeks, but < 1 year
  • Age < 18 years and > 50 years

Sites / Locations

  • Research Unit for General Practice, Department of gastroenterology, Odense University hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Positive diagnosis

Diagnosis of exclusion

Arm Description

The diagnosis of IBS is based on the international ROME III criteria, few blod tests, and abscence of danger signals

The diagnosis of IBS is based on normal extended blood tests, screening for celiac sprue and lactose intolerance, stool for ova and parasites and endoscopy with biopsy

Outcomes

Primary Outcome Measures

Health related quality of life

Secondary Outcome Measures

Findings of organic disease
We will look at the findings of organic disease (for example celiac disease or colorectal cancer) in the two investigation programes.

Full Information

First Posted
June 28, 2010
Last Updated
October 24, 2011
Sponsor
University of Southern Denmark
Collaborators
Mejeribrugets ForskningsFond, Arla Foods
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1. Study Identification

Unique Protocol Identification Number
NCT01153295
Brief Title
"Functional Bowel Disorder. Investigation in General Practice"
Official Title
"Functional Bowel Disorder. Investigation in General Practice"
Study Type
Interventional

2. Study Status

Record Verification Date
December 2008
Overall Recruitment Status
Completed
Study Start Date
December 2008 (undefined)
Primary Completion Date
June 2011 (Actual)
Study Completion Date
June 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern Denmark
Collaborators
Mejeribrugets ForskningsFond, Arla Foods

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The study aims to investigate how to give the diagnosis of Irritable Bowel Syndrome. The investigators compare two parallel groups of primary care patients, in the age of 18-50 years with gastrointestinal complaints where the GP suspects IBS. All included patients fulfil international diagnostic criteria (ROME III) and have no danger signals. Group 1: The diagnosis is based on the diagnostic criteria and few blod tests Group 2: The diagnosis is a diagnosis of exclusion after investigations with extended blod tests, examination for milk- and gluten intolerance, stoll for ova and parasites and scopy of the intestine. After receiving the diagnosis of Irritable bowel syndrome all patients are informed about the condition. The investigators follow the patients for 1 year. The investigators hypothesis is that the two investigation programmes (group 1 and 2)are equal with respect to the patients´ quality of life, symptoms and satisfaction and also with respect to finding of organic diseases.
Detailed Description
Background: Two opposing approaches can be distinguished in establishing the diagnosis of Irritable Bowel Syndrome (IBS): IBS as a "diagnosis of exclusion" versus IBS as a syndromic condition on its own. In Denmark we have no consensus on how to establish the diagnosis, but must often GPs approach IBS as a diagnosis of exclusion. Guidelines from the United Kingdom and the United States recommend the second approach, where the diagnosis is given as a positive diagnosis based on symptom-based IBS criteria. We lack research on this area carried out under controlled circumstances and in primary care in Denmark. Aim: To evaluate two investigation programmes for diagnosing IBS in primary care patients in Denmark. We want to compare the two programmes in relation to the effect on the patients´ symptoms, quality of life and satisfaction, and also the cost and safety when using the different programmes. Also we want to see how the GP´s understanding of IBS correlate with the IBS criteria (ROM I, II and III) Methods: A randomised, non-blinded, controlled intervention study of two parallel groups. The target group comprises people aged 18-50 years, who consult their GP with gastrointestinal complaints, where the GP suspects IBS and refers the patient to the study. To be included in the study the patients have to fulfil the ROM III criteria and they may not have any alarm signals. Included patients are randomised to one of two different investigation programmes, where the diagnosis is given as: A positive diagnosis, the diagnosis is based on the ROM III criteria and a few blood tests (FBC, CRP) A diagnosis of exclusion, the diagnosis is given after normal investigation (extended blood tests, screening for celiac sprue and lactose intolerance, endoscopy) The patients are followed by means of monthly letters, with questions about current GI symptoms, sick-leave days, visits at GPs, use of medication etc., and validated questionnaires at baseline, after 4 weeks, 6 months and 12 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Irritable Bowel Syndrome
Keywords
IBS, Irritable bowel syndrome, diagnosis, safety, Health related quality of life

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
153 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Positive diagnosis
Arm Type
Experimental
Arm Description
The diagnosis of IBS is based on the international ROME III criteria, few blod tests, and abscence of danger signals
Arm Title
Diagnosis of exclusion
Arm Type
Active Comparator
Arm Description
The diagnosis of IBS is based on normal extended blood tests, screening for celiac sprue and lactose intolerance, stool for ova and parasites and endoscopy with biopsy
Intervention Type
Procedure
Intervention Name(s)
Clinical diagnosis based on symptom criteria
Intervention Description
The diagnosis is based on ROME III criteria, abscence of danger signals and FBC, CRP
Intervention Type
Procedure
Intervention Name(s)
Diagnosis of exclusion
Intervention Description
The diagnosis is based on normal investigations involving endoscopy with biopsy, stool for ova and parasites, FBC, CRP, TSH, Ca, ALT, alanine aminotransferase; alkaline phosphatase, serum bilirubin, Screening for lactose and celiac sprue
Primary Outcome Measure Information:
Title
Health related quality of life
Time Frame
One year
Secondary Outcome Measure Information:
Title
Findings of organic disease
Description
We will look at the findings of organic disease (for example celiac disease or colorectal cancer) in the two investigation programes.
Time Frame
one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Fulfill ROME III criteria age 18-50 years signed informed content Exclusion Criteria: Danger signals (fever, anaemia, weightloss, blod in stools, predisposition for CRC or IBD) abnormal physical examination comorbidity abuse lacking ability to talk and understand danish pregnancy Performed endoscopy within the last 3 years For patients > 40 years. Changed bowel habits, with duration > 3 weeks, but < 1 year Age < 18 years and > 50 years
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ove B. Schaffalitzky de Muckadell, Professor
Organizational Affiliation
Odense University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Research Unit for General Practice, Department of gastroenterology, Odense University hospital
City
Odense
ZIP/Postal Code
5000
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
33029843
Citation
Engsbro AL, Begtrup LM, Haastrup P, Storsveen MM, Bytzer P, Kjeldsen J, Schaffalitzky De Muckadell O, Jarbol DE. A positive diagnostic strategy is safe and saves endoscopies in patients with irritable bowel syndrome: A five-year follow-up of a randomized controlled trial. Neurogastroenterol Motil. 2021 Mar;33(3):e14004. doi: 10.1111/nmo.14004. Epub 2020 Oct 7.
Results Reference
derived
PubMed Identifier
23357491
Citation
Begtrup LM, Engsbro AL, Kjeldsen J, Larsen PV, Schaffalitzky de Muckadell O, Bytzer P, Jarbol DE. A positive diagnostic strategy is noninferior to a strategy of exclusion for patients with irritable bowel syndrome. Clin Gastroenterol Hepatol. 2013 Aug;11(8):956-62.e1. doi: 10.1016/j.cgh.2012.12.038. Epub 2013 Jan 26.
Results Reference
derived

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"Functional Bowel Disorder. Investigation in General Practice"

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