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Study of Gastric Motility in Eosinophilic Gastritis
NCT05229432 · View on ClinicalTrials.gov ↗
Study Summary
Purpose: The study is a cross-sectional observational study designed to determine if eosinophilic gastritis (EG) results in gastric motility impairment. Hypothesis: Gastric dysfunction occurs in the natural history of EG but is underdiagnosed due, in part, to contraindications to the use of the standard meals used in gastric emptying studies.
Conditions Studied
Study Locations (3)
Illinois
- Northwestern University — Chicago
Maryland
- The National Institutes of Health — Bethesda
Utah
- University of Utah — Salt Lake City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2023-01-25 |
| Est. Completion | 2026-12-01 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05229432
The ClinicalTrials.gov registry entry for NCT05229432 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Children's Hospital Medical Center, Cincinnati, which has 715 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Gastroparesis appearing as the primary indexed condition, and to 0 interventions. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05229432 reports 3 study locations spanning 3 distinct geographic areas — top geographies include Illinois, Maryland, Utah. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05229432 about?
NCT05229432 is a clinical study titled "Study of Gastric Motility in Eosinophilic Gastritis". Purpose: The study is a cross-sectional observational study designed to determine if eosinophilic gastritis (EG) results in gastric motility impairment. Hypothesis: Gastric dysfunction occurs in the natural history of EG but is underdiagnosed due, in part, to contraindications to the use of the s...
What is the current status of trial NCT05229432?
This trial is currently recruiting. The enrollment target is 30 participants. The study started on 2023-01-25. Estimated completion is 2026-12-01.
What conditions does trial NCT05229432 study?
This clinical trial studies the following conditions: Gastroparesis, Eosinophilic Gastritis, Gastric Motility Disorder. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
Who is sponsoring clinical trial NCT05229432?
This trial is sponsored by Children's Hospital Medical Center, Cincinnati, which has 715 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05229432 being conducted?
This trial has 3 study locations across Illinois, Maryland, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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