Actively Recruiting
Oxygenation in Vascular Lesions of the Colon Comparing People With Acquired Vascular Abnormalities and Healthy Controls
Led by University of Chicago · Updated on 2025-06-10
30
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying oxygen levels in the colon of people who have acquired vascular abnormalities in the proximal colon, such as angiodysplasia, arteriovenous malformations, and hemangiomas. These lesions are often found in older adults and those with heart, lung, or kidney conditions, and they may cause bleeding or iron deficiency anemia. The study aims to understand whether chronic low oxygen levels contribute to these vascular lesions by comparing affected individuals to healthy controls. Participants are divided into two groups: those with vascular abnormalities in the proximal colon and those with healthy colons. Researchers will measure oxygen saturation in five locations within the proximal colon mucosa during standard colonoscopy procedures. This study is non-randomized and does not involve blinding. The main evaluation will track colonic oxygen saturation levels from baseline up to 12 months. During the study, participants will undergo colonoscopies as part of their standard care, where oxygen levels in the colon will be quantitatively measured. The team will monitor oxygen saturation to understand the role of oxygenation in these lesions. Participants may be followed for up to one year to assess changes over time. The trial is open to adults aged 18 to 89 years, including both those with vascular lesions and healthy volunteers.
CONDITIONS
Brief Title
Oxygenation in Vascular Lesions of the Colon
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Undergo standard of care colonoscopy
- Have a history of vascular lesions of the colon
- Have a healthy colon
- Be between 18 and 89 years of age
You will not qualify if you...
- Age less than 18 years
- Age greater than 90 years
- Have ulcerations in the ascending colon opposite the ileocecal valve
- Have had previous colon surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 12 months
Participants undergo measurements of oxygen levels in the proximal colon during standard of care colonoscopy.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
University of Chicago
Chicago, Illinois, United States, 60637
Actively Recruiting
Research Team
J
Joel Pekow, MD
K
Kristi Kearney, RN
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
SCREENING
Number of Arms
2
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