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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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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.

Finland1 site
  • Turku University Hospital

    Turku, 20521

Other trials in Finland

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)

  1. 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
  1. 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,
  2. PET tracer is 18 F-FDG, dose 280 megabequerel (MBq, bowel imaging)
  3. 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):
  1. T2 (field echo type) cor and ax
  2. T2
  3. T1 fs cor and ax +Gd
  4. T1 fs repeated (start at 40 seconds after injection)
  5. Diffusion
  6. 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)
  1. Number of study subjects 45
  2. Scanner PET/MRI
  3. 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..
  4. No quality issues (QA), routine radiological quality control
  5. The study has been accepted by the Ethical committee of Turku University Hospital
  6. Present study is academic study and all data relating to the study belongs to the investigators.
  7. The test patients are to undergo the study in September 2014. The study is to be started October 2014.
  8. 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 groups in NCT02364973
Study groupRoleWhat they receive
PET-MRIPatients 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.

  1. 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.

  1. First posted18 Feb 2015 (estimated)
  2. Study startNov 2014
  3. Primary completionDec 2019
  4. Study completionAug 2020

Resources

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)
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

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.

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