IBDNCT02364973
Combined PET-MRI in the Diagnostics of Chronic Inflammatory Bowel Diseases (IBD)- a Feasibility Study
An observational study of IBD, run by Turku University Hospital at 1 site in Finland.
Trial summary
The main purpose of the present study is to examine the diagnostic performance of combined PET-MRI in detecting colonic and small bowel wall inflammatory processes caused by ulcerative colitis and Crohn's disease. Read more about this study
- Who is it for?
- Ages 18 to 70 years
- Conditions the study is for
- IBD
- What is being tested?
- PET-MRI
- How many people
- 20 participants
- Where
- 1 siteFinland
- Study dates
- Nov 2014to Aug 2020
- 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 to 70 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: IBD patients living in the Turku University Hospital referral area
Who may be able to join
- age over 18 years
- IBD (ulcerative colitis or Crohn's disease diagnosed by endoscopy and/or radiology
- no previous abdominal surgery
- no biological therapy for IBD
Who cannot join
- pregnancy
- diabetes
- the patient is unable to give informed consent
Trial locations and contacts
1 site in 1 country.
About this study
The main purpose of the present study is to examine the diagnostic performance of combined PET-MRI in detecting colonic and small bowel wall inflammatory processes caused by ulcerative colitis and Crohn's disease.
Read the detailed description
COMBINED PET-MRI IN THE DIAGNOSTICS OF CHRONIC INFLAMMATORY BOWEL DISEASES (IBD)- A FEASIBILITY STUDY (RESEARCH CODE T31/2014)
- Background Ulcerative colitis and Crohn's disease are chronic inflammatory bowel diseases (IBD) with relapsing and remitting course. The incidence of IBD is highest in teenagers and young adults, but IBD may also affect children and old people. The diagnosis of IBD is based on clinical symptoms, endoscopy and histology of the bowel wall. Aims of the study The main purpose of the present study is to examine the diagnostic performance of combined PET-MRI in detecting colonic and small bowel wall inflammatory processes caused by ulcerative colitis and Crohn's disease. The hypothesis of the study is a) IBD-related inflammatory changes are detected by PET-MRI (18 F-FDG) and correlate with the endoscopic and histologic activity of colitis and ileitis. Study design A total of 45 IBD patients (ulcerative colitis or Crohn's disease) aged over 15 years will be recruited from the patients visiting outpatient gastroenterology clinic of Turku University Hospital. Every patient undergoes colonoscopy with biopsy specimens, endoscopic and histologic data are recorded via structured forms. Laboratory specimens with samples for biobank are obtained. Then the patients are examined by abdominal MRI and PET. Inclusion criteria:
- informed consent obtained
- age over 18 years
- diagnosis of ulcerative colitis or Crohn's colitis based on endoscopy and histology
- the activity of colitis confirmed by histology and/or elevated fecal calprotectin concentration
- fertile women have contraception
- no previous abdominal surgery
- no X-ray investtigations during preceding year
- Investigators Principal investigator Markku Voutilainen, MD, Department of Gastroenterology Other investigators Hannu Aronen, Sami Kajander, Johanna Virtanen, Virva Saunavaara, Department of Radiology and PET center. Mervi Tenhami, Saila Kauhanen, Department of surgery Pirjo Nuutila, Department of Endocrinology and PET center Jukka Kemppainen, physicist, PET center Olli Carpen, Department of pathology Ville Aalto, statistician, University of Turku,
- PET tracer is 18 F-FDG, dose 280 megabequerel (MBq, bowel imaging)
- Data of scans and details of scanning time (including positioning and transmission) by tracer, blood sampling (activity, metabolites)
- Before scanning: oral contrast intake (Mannitol dilution) 65 min
- Magnetic resonance imaging (MRI) positioning (prone position) 5min
- Abdominal MRI Scanning: 50min
- Region: from diaphragma to symphysis
- During the scan: i.v. Buscopan and +Gadolinium
- Sequences (fast gradient echo, predominantly breath-hold imaging):
- T2 (field echo type) cor and ax
- T2
- T1 fs cor and ax +Gd
- T1 fs repeated (start at 40 seconds after injection)
- Diffusion
- T2 or T1 cor +aks
- PET, FDG tracer: 15 min
- Total scanning time including positioning, MRI and PET: 70 min Scanning code JN5JS (= Large scale PET-MRI of the body)
- Number of study subjects 45
- Scanner PET/MRI
- The radiation dose will be calculated by physicist after the tracer, it's amount and detector are determined. The permission from ethical committee was obtained in August 2014..
- No quality issues (QA), routine radiological quality control
- The study has been accepted by the Ethical committee of Turku University Hospital
- Present study is academic study and all data relating to the study belongs to the investigators.
- The test patients are to undergo the study in September 2014. The study is to be started October 2014.
- For the financing of the study, VTR-/EVO-funding (Funding from the Finnish government) will be applied. At present, 6000€ have been obtained from research funding of Department of internal medicine.
- Conditions
- IBD
- Being tested
- PET-MRI
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PET-MRIOther
The study patients undergo positron emission tomography (PET) after informed consent is obtained
| Study group | Role | What they receive |
|---|---|---|
| PET-MRI | Patients with chronic inflammatory bowel disease who are treated at Turku University hospital outpatient clinic or ward Receives: Other: PET-MRI |
What is being measured
The primary outcome is the main question the study is designed to answer.
The percentage of patients with active inflammation detected by PET-MRI
COMBINED PET-MRI IN THE DIAGNOSTICS AND FOLLOW-UP OF CHRONIC INFLAMMATORY BOWEL DISEASES
Measured: 3 YEARS
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Feb 2015 (estimated)
- Study startNov 2014
- Primary completionDec 2019
- Study completionAug 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for IBDStudies of the same condition, open and under way.
- More trials run by Turku University HospitalThe sponsor's other registered studies.
- 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 only
- Time perspective
- Prospective
- Enrolment
- 20 participants (actual)
Sponsor and investigators
- Lead sponsor
- Turku University Hospital
- Sponsor type
- Other government
- Responsible party
- Sponsor
- Investigators
- Markku Voutilainen, MD, Principal investigator, Turku University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02364973
- Sponsor's protocol ID
- T31/2014
- Status last verified
- Mar 2021
- First submitted
- 3 Dec 2014
- Last updated
- 1 Apr 2021
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 1 Apr 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Combined PET-MRI in the Diagnostics of Chronic Inflammatory Bowel Diseases (IBD)- a Feasibility Study
- ClinicalTrials.gov ID
- NCT02364973
- Acronym / sponsor ID
- T31/2014
- Conditions
- IBD
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 20 participants (actual)
- Lead sponsor
- Turku University HospitalOther government
- Study start
- Nov 2014 (actual)
- Primary completion
- Dec 2019 (actual)
- Study completion
- Aug 2020 (actual)
- First posted
- 18 Feb 2015 (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 main purpose of the present study is to examine the diagnostic performance of combined PET-MRI in detecting colonic and small bowel wall inflammatory processes caused by ulcerative colitis and Crohn's disease.
Detailed description
COMBINED PET-MRI IN THE DIAGNOSTICS OF CHRONIC INFLAMMATORY BOWEL DISEASES (IBD)- A FEASIBILITY STUDY (RESEARCH CODE T31/2014)
- Background Ulcerative colitis and Crohn's disease are chronic inflammatory bowel diseases (IBD) with relapsing and remitting course. The incidence of IBD is highest in teenagers and young adults, but IBD may also affect children and old people. The diagnosis of IBD is based on clinical symptoms, endoscopy and histology of the bowel wall. Aims of the study The main purpose of the present study is to examine the diagnostic performance of combined PET-MRI in detecting colonic and small bowel wall inflammatory processes caused by ulcerative colitis and Crohn's disease. The hypothesis of the study is a) IBD-related inflammatory changes are detected by PET-MRI (18 F-FDG) and correlate with the endoscopic and histologic activity of colitis and ileitis. Study design A total of 45 IBD patients (ulcerative colitis or Crohn's disease) aged over 15 years will be recruited from the patients visiting outpatient gastroenterology clinic of Turku University Hospital. Every patient undergoes colonoscopy with biopsy specimens, endoscopic and histologic data are recorded via structured forms. Laboratory specimens with samples for biobank are obtained. Then the patients are examined by abdominal MRI and PET. Inclusion criteria:
- informed consent obtained
- age over 18 years
- diagnosis of ulcerative colitis or Crohn's colitis based on endoscopy and histology
- the activity of colitis confirmed by histology and/or elevated fecal calprotectin concentration
- fertile women have contraception
- no previous abdominal surgery
- no X-ray investtigations during preceding year
- Investigators Principal investigator Markku Voutilainen, MD, Department of Gastroenterology Other investigators Hannu Aronen, Sami Kajander, Johanna Virtanen, Virva Saunavaara, Department of Radiology and PET center. Mervi Tenhami, Saila Kauhanen, Department of surgery Pirjo Nuutila, Department of Endocrinology and PET center Jukka Kemppainen, physicist, PET center Olli Carpen, Department of pathology Ville Aalto, statistician, University of Turku,
- PET tracer is 18 F-FDG, dose 280 megabequerel (MBq, bowel imaging)
- Data of scans and details of scanning time (including positioning and transmission) by tracer, blood sampling (activity, metabolites)
- Before scanning: oral contrast intake (Mannitol dilution) 65 min
- Magnetic resonance imaging (MRI) positioning (prone position) 5min
- Abdominal MRI Scanning: 50min
- Region: from diaphragma to symphysis
- During the scan: i.v. Buscopan and +Gadolinium
- Sequences (fast gradient echo, predominantly breath-hold imaging):
- T2 (field echo type) cor and ax
- T2
- T1 fs cor and ax +Gd
- T1 fs repeated (start at 40 seconds after injection)
- Diffusion
- T2 or T1 cor +aks
- PET, FDG tracer: 15 min
- Total scanning time including positioning, MRI and PET: 70 min Scanning code JN5JS (= Large scale PET-MRI of the body)
- Number of study subjects 45
- Scanner PET/MRI
- The radiation dose will be calculated by physicist after the tracer, it's amount and detector are determined. The permission from ethical committee was obtained in August 2014..
- No quality issues (QA), routine radiological quality control
- The study has been accepted by the Ethical committee of Turku University Hospital
- Present study is academic study and all data relating to the study belongs to the investigators.
- The test patients are to undergo the study in September 2014. The study is to be started October 2014.
- For the financing of the study, VTR-/EVO-funding (Funding from the Finnish government) will be applied. At present, 6000€ have been obtained from research funding of Department of internal medicine.
Study design
- Observational model
- Case only
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| PET-MRI | – | Other: PET-MRIPatients with chronic inflammatory bowel disease who are treated at Turku University hospital outpatient clinic or ward |
Who may qualify
- Ages
- 18 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- IBD patients living in the Turku University Hospital referral area
Key inclusion criteria (4 listed)
- age over 18 years
- IBD (ulcerative colitis or Crohn's disease diagnosed by endoscopy and/or radiology
- no previous abdominal surgery
- no biological therapy for IBD
Key exclusion criteria (3 listed)
- pregnancy
- diabetes
- the patient is unable to give informed consent
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| PET-MRIThe study patients undergo positron emission tomography (PET) after informed consent is obtained | Other | PET-MRI |
Primary outcome
The percentage of patients with active inflammation detected by PET-MRI
Time frame: 3 YEARS
COMBINED PET-MRI IN THE DIAGNOSTICS AND FOLLOW-UP OF CHRONIC INFLAMMATORY BOWEL DISEASES
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 1 Apr 2021.
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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.
Markku Voutilainen, MD principal investigator
Turku University Hospital
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 IBD, run by Turku University Hospital at 1 site in Finland.
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 4 inclusion and 3 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 1 Apr 2021. 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 Finland. 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?
The percentage of patients with active inflammation detected by PET-MRI (time frame: 3 YEARS). 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 1 Apr 2021; AzTrials last refreshed its copy on 8 Nov 2026.