Clinical Trials in the USA / NCT05774080
Active, not recruiting
Observational
An Observational Study of Patients With Chronic Gastrointestinal Disease
NCT05774080 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Gastrointestinal Diseases
Investigational drug(s) / intervention(s)
Observational
Observational: Observational
Study summary
TARGET-GASTRO is an observational research study to conduct a comprehensive review of outcomes for patients with the chronic gastrointestinal (GI) diseases: eosinophilic gastrointestinal disease (EGID), ulcerative colitis (UC) or Crohn's disease (CD).
Eligibility
Disease Cohort
Inclusion Criteria:
* Adult\* patients at the time of enrollment with a diagnosis or major symptom of EGIDs, UC, or CD by ICD-10 code in the EHR interface
Exclusion Criteria:
* Death
* Manual removal (sponsor or site request)
* No EHR interface encounter \> 3 years.
Engaged Cohort
Inclusion Criteria:
* Adult\* patients diagnosed and managed for these conditions invited to participate
* Ability to provide written informed consent
Exclusion Criteria:
* Patient expressed desire to withdraw consent to complete PROs
* Failure to complete PROs within 24 weeks of initial invitation
* Greater than 24 months lapse of survey completion after baseline surveys completed
* Additionally, the criteria detailed for Disease Cohort apply to the Engaged Cohort.
Primary outcome measure(s)
- To characterize the natural history of disease in patients with GI disease from various etiologies — 20 Years
- To assess safety and effectiveness of treatments — 20 Years
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Atrium Health/Wake Forest University School of Medicine | Winston-Salem | North Carolina |
More Target PharmaSolutions, Inc. trials in the USA
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An Observational Study of Patients With Chronic Liver Disease
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Other trials for the same condition
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05774080 on ClinicalTrials.gov ↗ ← All trials in the USA