Inflammatory Bowel DiseaseNCT02255019
MRI in Patients With Inflammatory Bowel Disease
An observational study of Inflammatory Bowel Disease, run by Copenhagen University Hospital at Herlev at 1 site in Denmark.
Trial summary
The aim of this study is to find an optimal magnetic resonance imaging (MRI) method to examine patients with inflammatory bowel disease (IBD). Patients should furthermore avoid being exposed to unnecessary X-rays and invasive examination. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Inflammatory Bowel Disease
- How many people
- 125 participants
- Where
- 1 siteDenmark
- Study dates
- May 2011to Jun 2013
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Minimum 77 subjects in study I-V and minimum 15 subjects in the pilot study are included. All patients should eighter have a known IBD diagnose or suspect IBD. There will not be considered healthy subjects. Participants must be over 18 years old.
Who may be able to join
- patients with known or suspected IBD
- age > 18 years
Who cannot join
- age < 18 years
- low kidney function (eGFR < 30)
- contraindication for MRI (pacemaker, metal in the body, claustrophobia)
- dementia
- severe illness
- pregnancy/lactation
Trial locations and contacts
1 site in 1 country.
About this study
The aim of this study is to find an optimal magnetic resonance imaging (MRI) method to examine patients with inflammatory bowel disease (IBD). Patients should furthermore avoid being exposed to unnecessary X-rays and invasive examination.
It is the investigators expectation that this study will benefit to future patients, as they will be offered MRI as the first choice. Hereby, the patients avoid the risks and discomfort associated with x-ray examinations. The aim is that patients with IBD achieve better and earlier treatment and if this is achieved it both benefits patient and public health. An earlier treatment leads to fewer hospitalizations and thereby saving the community money.
The investigators hope is that the investigators study will show that MRI is one of the best tool to examine patients with IBD and that this in future leads MRI to be the first choice in contrary to all examinations with x-ray exposer, unless there is any contraindication to MRI.
Read the detailed description
IBD is a common term for two chronic diseases, Crohn's disease (CD) and ulcerative colitis (UC). IBD occurs often between the ages of 20-30 years. There are about 25,000 people in Denmark with IBD and diseases incidence and prevalence has increased over the past 20 years [1]. In Denmark, the incidence of CD increased fourfold to 10 per 100,000 inhabitants per years and the incidence of UC doubled to 17 per 100,000 inhabitants per years [2]. Its causes are not completely known but it indicates an interaction between genetic and external factors.
IBD as mentions is a chronic disease which means that it flare up periodically throughout life. Studies show that about 50% at a given time is in clinical remission, 25% had moderate disease activity and 25% have significant disease activity [3]. This means that patients with IBD are more likely to undergo repeatedly examinations to confirm or invalidate disease activity. It is essential for patients that the disease is kept under control so they can maintain a normal working life and a well-functioning social life.
Most studies as when the investigators study began have been in the form of conventional small-bowel follow-through and computed tomographic (CT). A few places in Denmark are beginning to experiment with MRI diagnostics but the method has still no standardized protocol.
There are many advantages by using MRI:
Patients avoid being exposed to X-ray radiation and thus the examination can be carried out repeatedly without any problems. It is especially important for fertile women.
There is no evidence of harmful effects of MRI as opposed to CT scanning, where repeated exposure to X-ray radiation increases the risk of cancer [4].
You could potentially avoid more invasive procedures, thus reducing study duration.
General requested the following highlighted in this project:
Compare the three different MRI scans Compare the clinic with MRI: Calprotectin compared with MRI findings.
The investigators will examine the following hypotheses:
MR enterography can diagnose pathology as well as or better than MRI enteroclysis.
Plain MRI can diagnose pathology as well as or better than MRI enteroclysis. Plain MRI can diagnose pathology as well as or better than MRI enterography.
Method:
This study is carried out as a prospective cross-sectional study (study I-V and a pilot study) in collaboration between radiology department and gastroenterology department at Herlev Hospital. The study recruit both inpatients and outpatients with known or suspected IBD. The main study will include at least 77 patients, while pilot study will include a minimum of 15 patients. Two experienced radiologists in the diagnosis of diseases gastrointestinal will describe the MRI scans. Interpretation of MRI are performed according to a standard table. Studies I-III will be compared to evaluate effectiveness these studies.
Patients will receive a faeces sample kit the first day they meet to MRI. The sample should be taken two days after the MRI scan and sent through the mail. The sample should contain about 5-10 g of faeces and it will be analyzed by ELISA method for calprotectin. Calprotectin is a good marker for the degree of inflammation in the intestines. [5] Analysis of each sample immediately after the reception is too costly. The samples are therefore frozen on the gastroenterology department at Herlev Hospital. When the investigators have collected about 20 samples which is expected to do within one month the samples are analyzed for calprotectin. The material are destroyed immediately after the analysis and can not be used in future research projects.
The study was approved by the Local Committee for Health Research Ethics and the Danish Data Protection Agency.
Study I: Plain MR: Patients undergoing an MRI of the abdomen without oral or IV contrast agent [6]. There are several new studies that show that the diffusion-weighted MRI is good at showing pathology [7-9]. Intravenous buscopan is given in all the studies to reduce peristalsis in the intestines during scan.
Study II: MR enterography: This study is done immediately after study I. Patients from the study I must then take approximately 1.5 l VoLume orally over 1 hour. Previous studies have shown that water alone, taken orally is absorbed very quickly in the intestines and thus does not result in the desired dilation [10-11].
VoLume is an aqueous solution of barium sulfate and it is not reabsorbed by the intestine. The contrast has no immediate side effects, it may in some cases cause constipation. It is crucial for the interpretation of MRI to achieve an optimal dilatation of the intestines. In the end of the scan patients get iv gadolinium. MR enterography is the gold standard in this study.
Study III: MR Enteroclysis (MRE): The above patients will undergo MRE approx. 7 days later. A nasojejunal tube will in placed under fluoroscopy. The radiation that patients are exposed to is minimal and without risk [11-12].
For study II and III should be comparable, it is important that the same amount of fluid is consumed in both studies.
Study IV: This part of the study will consist of a questionnaire-based study of the above patients' experience of the studies II-III [13].
Study V: In this study the calprotectin is compared with study II.
Study VI: Conducted as a pilot study. A small group of patients undergoing an MRI scan with IV contrast, as in substudy II, albeit without prior intake of 1.5 l barium solution. These patients also have an MRI enterografi (which substudy II) 3-7 days later. The results from these two scans are compared.
The study does not include operational or other interventional procedures on the patients involved in the study, and will not be used placebo.
Subjects Minimum 77 subjects in study I-V and minimum 15 subjects in the pilot study are included. All patients should eighter have a known IBD diagnose or suspect IBD. There will not be considered healthy subjects. Participants must be over 18 years old.
- Conditions
- Inflammatory Bowel Disease
- Medical subject headings
- Inflammatory Bowel Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| IBD, CD, UC | All patients should either have a known IBD diagnose or suspect of having IBD. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Inflammation changes in gastrointestinal tract in MRI.
Observe the inflammatory changes in bowel.
Measured: 1 day
evaluate MRI using faecal calprotectin (fC) as a reference standard.
MRI is evaluated and fC is received about 3 day after MRI.
Measured: 1-3 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Oct 2014 (estimated)
- Study startMay 2011
- Primary completionJun 2013
- Study completionJun 2013
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Inflammatory Bowel DiseaseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case crossover
- Time perspective
- Prospective
- Enrolment
- 125 participants (actual)
Sponsor and investigators
- Lead sponsor
- Copenhagen University Hospital at Herlev
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Kayalvily J. Nielsen, MD, Principal investigator, Copenhagen University Hospital at Herlev
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02255019
- Sponsor's protocol ID
- H-2-2010-149
- Status last verified
- Sep 2014
- First submitted
- 30 Sep 2014
- Last updated
- 2 Oct 2014
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 2 Oct 2014. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- MRI in Patients With Inflammatory Bowel Disease
- ClinicalTrials.gov ID
- NCT02255019
- Acronym / sponsor ID
- H-2-2010-149
- Conditions
- Inflammatory Bowel Disease
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 125 participants (actual)
- Lead sponsor
- Copenhagen University Hospital at HerlevUniversity, hospital or other
- Study start
- May 2011
- Primary completion
- Jun 2013 (actual)
- Study completion
- Jun 2013 (actual)
- First posted
- 2 Oct 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of this study is to find an optimal magnetic resonance imaging (MRI) method to examine patients with inflammatory bowel disease (IBD). Patients should furthermore avoid being exposed to unnecessary X-rays and invasive examination.
It is the investigators expectation that this study will benefit to future patients, as they will be offered MRI as the first choice. Hereby, the patients avoid the risks and discomfort associated with x-ray examinations. The aim is that patients with IBD achieve better and earlier treatment and if this is achieved it both benefits patient and public health. An earlier treatment leads to fewer hospitalizations and thereby saving the community money.
The investigators hope is that the investigators study will show that MRI is one of the best tool to examine patients with IBD and that this in future leads MRI to be the first choice in contrary to all examinations with x-ray exposer, unless there is any contraindication to MRI.
Detailed description
IBD is a common term for two chronic diseases, Crohn's disease (CD) and ulcerative colitis (UC). IBD occurs often between the ages of 20-30 years. There are about 25,000 people in Denmark with IBD and diseases incidence and prevalence has increased over the past 20 years [1]. In Denmark, the incidence of CD increased fourfold to 10 per 100,000 inhabitants per years and the incidence of UC doubled to 17 per 100,000 inhabitants per years [2]. Its causes are not completely known but it indicates an interaction between genetic and external factors.
IBD as mentions is a chronic disease which means that it flare up periodically throughout life. Studies show that about 50% at a given time is in clinical remission, 25% had moderate disease activity and 25% have significant disease activity [3]. This means that patients with IBD are more likely to undergo repeatedly examinations to confirm or invalidate disease activity. It is essential for patients that the disease is kept under control so they can maintain a normal working life and a well-functioning social life.
Most studies as when the investigators study began have been in the form of conventional small-bowel follow-through and computed tomographic (CT). A few places in Denmark are beginning to experiment with MRI diagnostics but the method has still no standardized protocol.
There are many advantages by using MRI:
Patients avoid being exposed to X-ray radiation and thus the examination can be carried out repeatedly without any problems. It is especially important for fertile women.
There is no evidence of harmful effects of MRI as opposed to CT scanning, where repeated exposure to X-ray radiation increases the risk of cancer [4].
You could potentially avoid more invasive procedures, thus reducing study duration.
General requested the following highlighted in this project:
Compare the three different MRI scans Compare the clinic with MRI: Calprotectin compared with MRI findings.
The investigators will examine the following hypotheses:
MR enterography can diagnose pathology as well as or better than MRI enteroclysis.
Plain MRI can diagnose pathology as well as or better than MRI enteroclysis. Plain MRI can diagnose pathology as well as or better than MRI enterography.
Method:
This study is carried out as a prospective cross-sectional study (study I-V and a pilot study) in collaboration between radiology department and gastroenterology department at Herlev Hospital. The study recruit both inpatients and outpatients with known or suspected IBD. The main study will include at least 77 patients, while pilot study will include a minimum of 15 patients. Two experienced radiologists in the diagnosis of diseases gastrointestinal will describe the MRI scans. Interpretation of MRI are performed according to a standard table. Studies I-III will be compared to evaluate effectiveness these studies.
Patients will receive a faeces sample kit the first day they meet to MRI. The sample should be taken two days after the MRI scan and sent through the mail. The sample should contain about 5-10 g of faeces and it will be analyzed by ELISA method for calprotectin. Calprotectin is a good marker for the degree of inflammation in the intestines. [5] Analysis of each sample immediately after the reception is too costly. The samples are therefore frozen on the gastroenterology department at Herlev Hospital. When the investigators have collected about 20 samples which is expected to do within one month the samples are analyzed for calprotectin. The material are destroyed immediately after the analysis and can not be used in future research projects.
The study was approved by the Local Committee for Health Research Ethics and the Danish Data Protection Agency.
Study I: Plain MR: Patients undergoing an MRI of the abdomen without oral or IV contrast agent [6]. There are several new studies that show that the diffusion-weighted MRI is good at showing pathology [7-9]. Intravenous buscopan is given in all the studies to reduce peristalsis in the intestines during scan.
Study II: MR enterography: This study is done immediately after study I. Patients from the study I must then take approximately 1.5 l VoLume orally over 1 hour. Previous studies have shown that water alone, taken orally is absorbed very quickly in the intestines and thus does not result in the desired dilation [10-11].
VoLume is an aqueous solution of barium sulfate and it is not reabsorbed by the intestine. The contrast has no immediate side effects, it may in some cases cause constipation. It is crucial for the interpretation of MRI to achieve an optimal dilatation of the intestines. In the end of the scan patients get iv gadolinium. MR enterography is the gold standard in this study.
Study III: MR Enteroclysis (MRE): The above patients will undergo MRE approx. 7 days later. A nasojejunal tube will in placed under fluoroscopy. The radiation that patients are exposed to is minimal and without risk [11-12].
For study II and III should be comparable, it is important that the same amount of fluid is consumed in both studies.
Study IV: This part of the study will consist of a questionnaire-based study of the above patients' experience of the studies II-III [13].
Study V: In this study the calprotectin is compared with study II.
Study VI: Conducted as a pilot study. A small group of patients undergoing an MRI scan with IV contrast, as in substudy II, albeit without prior intake of 1.5 l barium solution. These patients also have an MRI enterografi (which substudy II) 3-7 days later. The results from these two scans are compared.
The study does not include operational or other interventional procedures on the patients involved in the study, and will not be used placebo.
Subjects Minimum 77 subjects in study I-V and minimum 15 subjects in the pilot study are included. All patients should eighter have a known IBD diagnose or suspect IBD. There will not be considered healthy subjects. Participants must be over 18 years old.
Study design
- Observational model
- Case crossover
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| IBD, CD, UC | – | –All patients should either have a known IBD diagnose or suspect of having IBD. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Minimum 77 subjects in study I-V and minimum 15 subjects in the pilot study are included. All patients should eighter have a known IBD diagnose or suspect IBD. There will not be considered healthy subjects. Participants must be over 18 years old.
Key inclusion criteria (2 listed)
- patients with known or suspected IBD
- age > 18 years
Key exclusion criteria (6 listed)
- age < 18 years
- low kidney function (eGFR < 30)
- contraindication for MRI (pacemaker, metal in the body, claustrophobia)
- dementia
- severe illness
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Inflammation changes in gastrointestinal tract in MRI.
Time frame: 1 day
Observe the inflammatory changes in bowel.
evaluate MRI using faecal calprotectin (fC) as a reference standard.
Time frame: 1-3 days
MRI is evaluated and fC is received about 3 day after MRI.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Oct 2014.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Kayalvily J. Nielsen, MD principal investigator
Copenhagen University Hospital at Herlev
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Inflammatory Bowel Disease, run by Copenhagen University Hospital at Herlev at 1 site in Denmark.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 2 Oct 2014. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Inflammation changes in gastrointestinal tract in MRI. (time frame: 1 day). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Oct 2014.