University of Chicago
Chicago, Illinois, 60637, United States
Location status: Recruiting
Location contact
Joel Pekow, MD
CONTACT
Kristi Kearney, RN
CONTACT
NCT Number: NCT06230731
The goal of this clinical trial is to evaluate oxygenation in the colon in people with acquired vascular abnormalities in the proximal colon.
Interested in participating?
Request Info18 year–89 year
All sexes
Interventional
Not applicable
Chicago, Illinois, 60637, United States
Location status: Recruiting
Joel Pekow, MD
CONTACT
Kristi Kearney, RN
CONTACT
The etiology of acquired vascular abnormalities of the large bowel (i.e. angiodysplasia, AVM, hemangiomas of the cecum. etc.) are unknown. These lesions typical appear as ectatic, dilated, and tortuous blood vessels within the submucosa and mucosa of the GI tract. In some patients they are the cause of acute large volume bleeding or a slower chronic bleed that manifests as chronic iron deficiency anemia. These lesions are more common in older individuals and those with underlying cardiac, pulmonary, and renal disease. As such, it is hypothesized that these lesions may result from chronic hypoxia. This study aims to evaluate oxygenation of the colon in people with acquired vascular abnormalities in the proximal colon compared to healthy controls.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Measure oxygen levels in 5 proximal colon mucosa locations.
Time frame: baseline-12 months
Colonic oxygen saturation levels will be compared between patients with vascular lesions of the colon and healthy controls.
Contact information is provided by the study sponsor or research team.
Joel Pekow, MD
CONTACT
Kristi Kearney, RN
CONTACT
University of Chicago
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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