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NCT07467980 · ClinicalTrials.gov registry record
Endoscopic COlorectal Mucosal Evaluation of Oxygen Tension
A clinical trial, sponsored by Vanderbilt University Medical Center.
- Recruiting
- Registry status
- 80
- Enrollment target
NCT07467980: Recruiting study, sponsored by Vanderbilt University Medical Center.
NCT07467980 is a clinical trial that is actively recruiting participants, run by Vanderbilt University Medical Center. The registered enrollment target is 80 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07467980 is actively recruiting participants, sponsored by Vanderbilt University Medical Center.
- RECRUITING
- Registry status
- 80 participants
- Enrollment target
Study Summary
Anastomosis refers to the surgical connection between two segments of the bowel, typically performed during colon and rectal surgeries to restore the continuity of the digestive tract after a section has been removed. It is necessary that the ends of the tissue at the anastomotic site are healthy (and capable of healing properly) as this will prevent dreaded complications like anastomotic leaks or strictures which can occur in almost a fifth of patients leading to increased hospital length of stay, costs, and mortality. Currently, the most widely used method for assessing tissue viability during anastomosis is indocyanine green fluorescence angiography (ICG-FA). This technique involves injecting a fluorescent dye (indocyanine green) into the bloodstream, which highlights blood flow and tissue perfusion under a special camera. However, ICG-FA has limitations due to allergies and reliability due to the dye's rapid disappearance from the bloodstream. Additionally, the dye cannot be administered repeatedly. This study explores a new method of measuring tissue oxygenation by evaluating mucosal oxygen saturation (StO2) as an alternative to ICG-FA. By evaluating StO2 levels, the research aims to provide a more reliable and repeatable way to assess tissue viability without the drawbacks of using fluorescent dyes. Secondly, any blood supply interruption to the bowel will first lead to mucosal ischemia, which can potentially be reliably captured by measuring mucosal StO2 levels only. In this single-center prospective single-arm study, we will evaluate whether mucosal StO2 levels are associated with or can predict anastomotic complications. This study will not involve any intervention that would affect the standard of care.
Primary Outcome
leaks and strictures
Interventions
- DEVICE A novel endoscopic imaging system that displays real-time oxygen saturation levels
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2026-03-16 |
| Est. Completion | 2028-04 |
What NCT07467980 shows while recruiting
NCT07467980 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 80 participants, a relatively small participant target.
The record links to 0 conditions, and to 1 intervention - of which A novel endoscopic imaging system that displays real-time oxygen saturation levels is the first listed.
NCT07467980 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT07467980 about?
NCT07467980 is a clinical study titled "Endoscopic COlorectal Mucosal Evaluation of Oxygen Tension". Anastomosis refers to the surgical connection between two segments of the bowel, typically performed during colon and rectal surgeries to restore the continuity of the digestive tract after a section has been removed. It is necessary that the ends of the tissue at the anastomotic site are healthy (a...
What is the current status of trial NCT07467980?
This trial is currently recruiting. The enrollment target is 80 participants. The study started on 2026-03-16. Estimated completion is 2028-04.
What interventions are being tested in trial NCT07467980?
The interventions under investigation include: A novel endoscopic imaging system that displays real-time oxygen saturation levels (DEVICE).
Who is sponsoring clinical trial NCT07467980?
This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.
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