MRI in Normal Ileal Pouches, and a Feasibility Study of Dynamic MRI Enema and Defaecating MRI Pouchography
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|ClinicalTrials.gov Identifier: NCT02925260|
Recruitment Status : Unknown
Verified August 2017 by London North West Healthcare NHS Trust.
Recruitment status was: Recruiting
First Posted : October 5, 2016
Last Update Posted : August 17, 2017
|Condition or disease||Intervention/treatment|
|Colitis, Ulcerative Ileal Pouches||Other: MRI with ileal pouch contrast and enema.|
Show Detailed Description
|Study Type :||Observational|
|Estimated Enrollment :||20 participants|
|Official Title:||Pelvic Collections on MRI in Patients With Ileal Pouches, and a Feasibility Study of Dynamic MRI Enema and Defaecating MRI Pouchography|
|Actual Study Start Date :||May 10, 2017|
|Estimated Primary Completion Date :||October 2017|
|Estimated Study Completion Date :||October 2017|
Patients with normal ileal pouches
Other: MRI with ileal pouch contrast and enema.
Pre enema 20mg IV or IM Hyoscine Butylbromide (Buscopan) Pre enema Small Field of View (SFOV) T2 sagittal series Pre enema SFOV T2 axial series Pre enema SFOV T1 sagittal series (fat suppressed) Pre enema SFOV T1 axial series (fat suppressed) Enema infiltration started During enema filling Dynamic T1 sagittal single image, fat suppressed, aligned on pouch-anal anastomosis During enema filling T1 sagittal series (fat suppressed) During enema filling T1 axial series (fat suppressed) Jelly infiltrated and held Evacuating series Oblique sagittal T2 evacuating series of the mid and distal pouch, aligned to the pouch-anal anastomosis
- The prevalence of pelvic collections in a representative sample of patients with normally functioning ileal pouches. [ Time Frame: Baseline ( MRI scan) ]
- A descriptive assessment of the normal variation of ileal pouches on MRI scans. [ Time Frame: Baseline ( MRI scan) ]
- Assess the patient experience of MRI pouchography using enemas [ Time Frame: Baseline ( MRI scan) ]Non-validated questionnaire assessment of patient anxiety, comfort, embarrassment and confidence in the outcome.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02925260
|Contact: Guy HT Worley, BMBS MRCS||+44 email@example.com|
|St Mark's Hospital||Recruiting|
|London, Middlesex, United Kingdom, HA1 3UJ|
|Contact: Guy Worley, BMedSci BMBS MRCS +4407984680155 firstname.lastname@example.org|
|Principal Investigator:||Guy HT Worley, BMBS MRCS||St. Mark's Hospital|
|Study Chair:||Susan K Clark, PhD||St. Mark's Hospital|