Assessing Barrett's Esophagus in Patients with Anorexia Nervosa and Purging Behaviors
Official title: Presence of Barrett's Esophagitis in a Cohort of People With Eating Disorders Who Engage in Purging Behaviors: A Pilot Study
Run by Denver Health and Hospital Authority · NCT06532734 · Data updated 2026-11-12
This study is trying to see if people with anorexia nervosa who purge have Barrett's esophagus, using non-invasive tests to check for this condition in patients aged 18-65.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 25 (estimated) |
| Sponsor | Denver Health and Hospital Authority Academic / other |
| Locations | 3 sites (Denver, Colorado and 2 other locations) |
| Status | Recruiting |
| Started | November 12, 2024 |
| Main results expected | November 2026 |
| Study ends | November 2026 |
| Registry record updated | December 10, 2025 |
| Trial ID | NCT06532734 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults aged 18-65 with a diagnosis of an eating disorder that includes a history of purging behaviors for five years or more.
✕Probably not a fit
Patients who do not have purging behaviors or those who are outside the age range of 18-65 will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to investigate the presence of Barrett's esophagus (BE) in individuals diagnosed with anorexia nervosa who exhibit purging behaviors, such as vomiting and rumination. It will utilize non-endoscopic testing methods to identify BE in a cohort that typically does not meet the standard screening guidelines. The study focuses on patients aged 18-65 with a history of purging for at least five years, who are admitted to a specialized center for eating disorders. By examining this population, the study seeks to provide insights into the prevalence of BE in younger patients with severe eating disorders.
Why it matters
Potential benefit: If successful, this study could lead to earlier detection and management of Barrett's esophagus in patients with eating disorders, potentially improving their long-term health outcomes.
How similar studies have gone: While there have been case reports on this topic, this study represents a novel approach as no comprehensive cohort studies have been conducted to assess Barrett's esophagus in this specific population.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients diagnosed with an eating disorder diagnosis that includes purging history * Ages 18-65 * Purging history =\>5 years * Purging or rumination at a minimum of once daily upon admission. * Admission to the ACUTE Center for Eating Disorders and Severe Malnutrition Exclusion Criteria: * Any eating disorder diagnosis that does not include purging behaviors * Ages under 18 and over 65 * Patients who otherwise meet the current ACG screening guidelines (chronic GERD and 3 or more risk factors for Barrett's mentioned in the Background) * Received mandated care at time of enrollment * Inability to consent to participate in the research
Where it's running
-
ACUTE Center for Eating Disorders and Severe Malnutrition
Denver, Colorado, United States Recruiting -
Denver Health and Hospital Authority
Denver, Colorado, United States Recruiting -
Denver Health and Hospital Authority
Denver, Colorado, United States Recruiting
Study contacts
- Principal investigator: Allison Nitsch, MD — Denver Health and Hospital Authority
- Study coordinator: Marina J Foster, BA
- Email: marina.foster@dhha.org
- Phone: 303-602-1913
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Itraconazole with endoscopic ablation to prevent esophageal cancer in high‑risk Barrett's esophagus
This study tests if adding itraconazole to the standard endoscopic ablation can better prevent esophageal cancer in people with high-risk Barrett's esophagus.
-
Detecting Barrett's Esophagus in Patients Without GERD Symptoms
This study is testing a new way to find Barrett's esophagus in people who don’t have GERD symptoms by using a simple capsule test instead of the usual endoscopy.
-
Using a swallowable sponge to collect esophageal samples for Barrett's esophagus detection
This study is testing a swallowable sponge to see if it can safely collect samples from the esophagus to help detect Barrett's esophagus and esophageal cancer in patients who may have these conditions.
-
Registry for patients undergoing esophageal cancer screening
This study is collecting information from patients getting screened for Barrett Esophagus and Esophageal Adenocarcinoma using a new test to see how well it works and how patients feel about the process.
-
Comparing surveillance and therapy for Barrett's esophagus with low-grade dysplasia
This study is testing whether regular check-ups or a treatment to remove precancerous cells is better for people with Barrett's esophagus and low-grade dysplasia.
-
Comparing biopsy methods for monitoring Barrett's Esophagus
This study is testing whether a new biopsy method called WATS is better than the usual random biopsies for monitoring patients with Barrett's Esophagus who are at high risk for serious complications.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.