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Prognostic Role of Bowel Ultrasound Scan in Children Affected by Acute Severe Colitis

Prognostic Role of Bowel Ultrasound Scan in Children Affected by Acute Severe Colitis (ASC): A Prospective Multicenter Study From the Paediatric IBD Porto Group of ESPGHAN

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06324500
Enrollment
120
Registered
2024-03-22
Start date
2020-03-02
Completion date
2025-05-02
Last updated
2024-03-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Severe Colitis

Brief summary

ASC is a life-threatening medical emergency. The lack of a timely intervention has shown to be associated with a mortality rate higher than 20% in adults, whereas a prompt targeted therapy has displayed a decrease of the aforementioned rate to 1%. Therefore, the identification of predictors of poor outcome trough an objective tool may provide crucial help to individualize the timing of second line treatment initiation. At the state of the art, PUCAI represents the only validated tool to appraise the risk of first-line treatment failure and there is a lack of objective methods with a prognostic value in ASC. BUS has proven to be a reliable tool in assessing disease activity in children with UC and it has also shown statistically significant correlation with endoscopic features of disease activity. Given the literature suggesting a role for BUS in severe UC and the results from our retrospective study we aim to validate our findings trough a prospective assessment of the potential prognostic role of BUS in ASC.

Interventions

None listed

Sponsors

Meyer Children's Hospital IRCCS
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Patients aged \< 18 years hospitalized for ASC with diagnosis of UC established by the presence of accepted clinical, radiologic, endoscopic, and histologic criteria

Exclusion criteria

* Patients with infectious colitis; * Patients undergoing treatment with anti-TNF alpha agents; * Patients already enrolled during the study period for a previous ASC attack;

Design outcomes

Primary

MeasureTime frameDescription
Colonic wall thickness of BUS (bowel ultrasound) parameter to predict the failure of first line treatmentWithin 48 hours from i.v. steroid treatment initiationInvestigation of the ability of BUS (bowel ultrasound) parameters, such as Colonic wall thickness (CWT) measured in mm, assessed within 48 hours from i.v. steroid treatment initiation, to predict the failure of first line treatment (defined according to the latest ESPGHAN guidelines). CWT will be measured from the edge of the outer wall to the inner echogenic lumen, containing air, or to the central echogenic mucosal stripe. CWT will be assessed as follows: two measurement through longitudinal plain and two through tranverse plain will be performed and the mean value (the sum of each measurement divided for 4) will be taken into account
Color and power Doppler vascularization of BUS (bowel ultrasound) parameter to predict the failure of first line treatmentWithin 48 hours from i.v. steroid treatment initiationColonic wall vascularization will be assessed according to the Limberg score to identify two subgroups: 1) increased vascularization (Limberg score 3-4); 2) normal colonic wall flow (Limberg Score 0-2). Such classification will be used, measured within the first 48 hours from i.v. steroid initiation, to predict failure of first line treatment (according to the latest ESPGHAN guidelines)
Mesenteric lymph nodes BUS (bowel ultrasound) parameterWithin 48 hours from i.v. steroid treatment initiationPresence of enlarged mesenteric lymph nodes, defined by short axis \> 5 mm it will be assessed within 48 hours from i.v. steroid treatment initiation, to predict the failure of first line treatment (defined according to the latest ESPGHAN guidelines)

Secondary

MeasureTime frameDescription
evaluation of the prognostic value of the ultrasound parametersWithin 48 hours from second-line therapy initiationevaluation of the prognostic value of the ultrasound parameters in predicting the possible failure of second-line therapy and therefore the need to carry out colectomy surgery

Countries

Italy, Spain

Contacts

Primary ContactPaolo Lionetti
paolo.lionetti@meyer.it3398416059
Backup ContactLuca Scarallo
luca.scarallo@meyer.it3928166681

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026