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High Dose Steroid Therapy to Treat Flares in Patients With Inflammatory Bowel Disease (IBD)

A Pilot Study Investigating the Feasibility and Efficacy of Locoregional Intra-arterial Administration of Methylprednisolone as a Bridge Therapy to Treat Symptomatic Flares in Inflammatory Bowel Disease

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05587673
Acronym
IBDIR
Enrollment
3
Registered
2022-10-20
Start date
2022-10-06
Completion date
2024-10-11
Last updated
2024-11-26

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

Conditions

Crohn Disease, Indeterminate Colitis, Inflammatory Bowel Diseases, Ulcerative Colitis

Brief summary

This study will examine whether delivery of high dose steroids, directly into the inflamed bowel via its arterial blood supply, will be better for treating uncontrolled flares of inflammatory bowel disease in patients compared to conventional intra-venous or oral administration of this drug. Patients aged 4-25 years of age will be recruited. In this study, the Investigator hopes to also learn how this directed steroid delivery during an active flare will improve patient symptoms as well as the appearance of inflamed segments of bowel determined by imaging or biopsy (i.e. at the time of endoscopy). Additional data will determine how the blood vessels in the bowel affect, and potentially even drive the mechanisms, of inflammatory bowel disease.

Interventions

DRUGMethylprednisolone

High dose steroid injected directly into the inflamed bowel segment(s) via its arterial blood supply.

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
4 Years to 25 Years
Healthy volunteers
No

Inclusion criteria

* Patients with newly diagnosis of inflammatory bowel disease (IBD) or patients who have an established diagnosis of IBD and are experiencing an acute flare which is not being controlled with first line therapy * Patients present with typical IBD symptoms which will include, but are not limited to, abdominal pain, loss of appetite, rectal bleeding, diarrhea, obstruction, or passage of mucus. * Patients referred by the GI team. * Patients (or guardians/parents) must be able and willing to give consent (or assent where applicable) and be able to attend all study visits.

Exclusion criteria

* Patients with MR unsafe metallic implants that will not be able to undergo the MRI portion of the study. * Patients with renal function impairment (GFR < 45 mL/min) preventing contrast administration. * Patients with contrast allergy.

Design outcomes

Primary

MeasureTime frameDescription
Number of patients with symptomatic, imaging or biopsy related improvement in their IBD symptomsBaseline through week 6Number of patients who have symptomatic, imaging or biopsy related improvement in their IBD symptoms following locoregional intraarterial methylprednisolone administration into the affected segment of bowel.

Secondary

MeasureTime frameDescription
Number of patients in which pre-procedural and procedural imaging can be correlated with clinical outcomes following therapyMonth 6Patients will have their pre-procedural and procedural imaging correlated with clinical outcomes following therapy.
Number of patients who have molecular changes correlated with improvement in symptoms following intraarterial steroid therapy.Month 6Number of patients who have molecular changes on their pre and post therapy biopsy which can be correlated with improvement in symptoms or imaging data from a patient.

Countries

United States

Outcome results

None listed

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