Non-Invasive Monitoring Through Bowel Ultrasound in Paediatric Inflammatory Bowel Disease Study
NCT ID: NCT05673278
Last Updated: 2023-08-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
50 participants
OBSERVATIONAL
2023-05-01
2024-05-01
Brief Summary
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Monitoring inflammation in this population currently is done with regular endoscopy (camera tests) and/ or MRI enterography scans which are invasive, can be uncomfortable, expensive and may have long waiting lists. These studies also require bowel prep, in the form of laxative medicines which can be distressing and cause time off from school. Direct visualisation through ultrasound could allow better monitoring of disease, and is quick, accurate, non-invasive and relatively low-cost. This could also allow for more appropriate medication use and a decrease in over/under use of medicines.
This study will aim to recruit 50 children and young people with inflammatory bowel disease. Each child will have an ultrasound scan after enrolment and the investigators will use the information from these scans, as well as routine blood tests (already taken in normal care) and follow up medical information to explore the use of ultrasound in this group. The investigating team will aim to contribute to the global discussion around this topic and if results are positive will aim to improve monitoring for this population managed at the Noah's Ark Children's Hospital for Wales.
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Detailed Description
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The null hypothesis in this study is that there is no association between gut ultrasound findings and blood and stool tests of inflammation or disease activity scores in paediatric patients with inflammatory bowel disease. The alternative hypothesis is that there is an association between ultrasound findings and these parameters. Regarding the follow up part of the study, the null hypothesis is that abnormal ultrasound findings have no correlation with either increase or decrease in treatment. The alternative hypothesis is that abnormal ultrasound findings correlate with increase in treatment and normal findings with no change or decrease in treatment.
A prospective feasibility observational methodology will be employed.
In terms of timetable for the study, preparation, including seeking of ethical and research and development alongside study logistics will be undertaken in the first 3 months. Participants will be recruited between months 4 and 18, with data collection and assessment over this time frame. Data will be analysed from months 6 to 24.
Recruitment of children will occur at a routine point of contact with paediatric gastroenterology services, i.e. inpatient review, outpatient attendance for infusion, clinic appointment or endoscopy, or through a virtual recruitment process, where deemed appropriate by the study team. Participants and their families will be provided with age-appropriate information and offered time to review these resources before obtaining consent. When recruited, study team will collect initial recruitment data, i.e. baseline characteristics. The investigating team will aim to arrange for ultrasound appointment as part of routine visit or during inpatient admission. On the day of ultrasound participants will attend the Noah's Ark children's hospital for Wales and scan will be undertaken. The trial team will review recent results (routine tests taken as part of normal care) at this point and then medical notes for clinical outcome up to twelve months after the scan. Results of project will be fed back to participants after study closure.
This project will be open to children with a diagnosis of IBD, according to the modified Porto criteria, aged between 2-19 years old. Only children without these diagnoses, those who have had surgery, which could act as a potential confounder in ultrasound findings, those outside of the age range and those belonging to families unable to give informed consent will be excluded. The information recorded from ultrasound scans will not be made available to the clinical team, therefore recruitment biases will be minimised. The target sample size of 50 children and young people has been set to achieve meaningful results and minimise statistical error. This figure is also based on other fledgling work in this area.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Children and young people diagnosed with inflammatory bowel disease aged 2-19 years
Diagnosis according to the modified Porto criteria All participants will undergo single ultrasound scan which will be evaluated with medical notes and results from routine care. No new samples will be taken outside of normal care.
Bowel Ultrasound Scan
Ultrasound scans will attempt to measure predefined criteria implemented in other research work using bowel ultrasound.
I - Bowel wall thickness II - Colour Doppler signal III - Loss of wall layer stratification IV - Loss of haustration V - Fatty wrapping VI - Motility in terminal ileum (TI) VII - Lymphadenopathy VIII - Abscess IX - Stricture
\+ Image quality
Interventions
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Bowel Ultrasound Scan
Ultrasound scans will attempt to measure predefined criteria implemented in other research work using bowel ultrasound.
I - Bowel wall thickness II - Colour Doppler signal III - Loss of wall layer stratification IV - Loss of haustration V - Fatty wrapping VI - Motility in terminal ileum (TI) VII - Lymphadenopathy VIII - Abscess IX - Stricture
\+ Image quality
Eligibility Criteria
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Inclusion Criteria
* Children with IBD, aged 2-19 years, diagnosed according to the modified Porto criteria
Exclusion Criteria
* Patients who have previously undergone bowel resection (subtotal colectomy, right hemicolectomy or stricturoplasty)
* Patients or families unable to give informed consent
* Children under 2 years of age or patients older than 19 years
2 Years
19 Years
ALL
No
Sponsors
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Cardiff and Vale University Health Board
OTHER_GOV
Responsible Party
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Principal Investigators
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Martin O Edwards, PhD FRCPCH
Role: PRINCIPAL_INVESTIGATOR
Cardiff and Vale University Health Board
Locations
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Noah's Ark Children's Hospital for Wales
Cardiff, , United Kingdom
Countries
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Central Contacts
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Facility Contacts
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References
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Green Z, Towriss C, Ashton JJ, Beattie RM, Evans A, Wahid A, Edwards M. Noninvasive monitoring with bowel ultrasound (NIMBUS) in paediatric inflammatory bowel disease: Feasibility in a single centre. J Pediatr Gastroenterol Nutr. 2025 Oct;81(4):1014-1023. doi: 10.1002/jpn3.70159. Epub 2025 Jul 21.
Green Z, Mayberry E, Ashton JJ, Beattie RM, Evans A, Wahid A, Edwards MO. NIMBUS study protocol: a single-centre feasibility study of non-invasive monitoring with bowel ultrasound in paediatric inflammatory bowel disease. BMJ Open. 2023 Dec 14;13(12):e078675. doi: 10.1136/bmjopen-2023-078675.
Other Identifiers
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8497/OCT/2022
Identifier Type: -
Identifier Source: org_study_id
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