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Anastomotic Leak Rectume-COMETNCT07467980

Endoscopic COlorectal Mucosal Evaluation of Oxygen Tension

An observational study of Anastomotic Leak Rectum and Anastomotic Leak Large Intestine, run by Vanderbilt University Medical Center at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
A novel endoscopic imaging system that displays real-time oxygen saturation levels
Type of treatment
Medical device
How many people
80 participants
Where
1 siteUnited States
Study dates
16 Mar 2026to Apr 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients meeting the eligibility criteria will be enrolled from the institution's colorectal surgery clinic in Nashville, TN

Who may be able to join

  • Adult patients (≥18 years).
  • Undergoing a colo-rectal anastomosis.
  • Patients who consent to study participation

Who cannot join

  • Patients undergoing a revision surgery.
  • Participants with missing data.
  • Patients who do not undergo intraoperative ICG-FA and StO2 endoscopic imaging promptly after the formation of a viable anastomosis.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

United States1 site, 1 recruiting
  • Vanderbilt University Medical Center

    Nashville, Tennessee, 37212

    Vanderbilt Colon and Rectal Surgery, (615) 322-2063, aimal.khan@vumc.org

    Recruiting

Other trials in United States

About this study

Official title: Anastomotic Site Mucosal Oxygen Tension and Its Association With Anastomotic Complications

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.

Read the detailed description

Virtually all patients undergoing elective colon and rectal resections undergo bowel anastomosis. These surgeries are often technically challenging, with significant morbidity and mortality in the case of an anastomotic leak, which can affect up to 21% of patients. In addition to increased morbidity and mortality, anastomotic leaks are associated with increased hospital length of stay and cost. Anastomotic leak following colon and rectal surgery is multifactorial, involving an intimate interplay of patient-related, tumor, and surgical risk factors. While decreased perfusion to anastomosis plays a central role in its pathophysiology. Poor perfusion at the anastomotic site can also lead to anastomotic strictures - requiring further reoperations , and in some cases, be equally catastrophic as anastomotic leaks.

As such, multiple attempts have been made to reduce the incidence of leaks. It is believed that the ability to accurately determine intraoperative tissue perfusion and oxygenation can help reduce the incidence of anastomotic leaks. Investigators have explored multiple modalities and benchmarks in human and animal models over the past three decades; these include colonic coloration, mesenteric pulsations, tissue perfusion using Doppler ultrasound quantitative visual analysis of tissue oxygenation using either indocyanine green or non-contrast tissue oxygenation imaging tools to detect predictors of anastomotic leak and hyperbaric oxygenation in mice models to improve anastomotic healing. While a few studies have found an association between low tissue oxygen tension and anastomotic leak development, there have only been a handful of large-scale human studies.

Currently, indocyanine green fluorescence angiography (ICG-FA) is the most widely accepted in this regard. It has shown a significant reduction in anastomotic leaks owing to a change in the resection margin. However, ICG-FA is contraindicated in patients with a history of contrast allergy. It also has a higher plasma disappearance, leading to an unstable fluorescence signal for the estimation of tissue congestion, causing reduced precision in estimates and an introduction of subjectivity and reduced standardization; furthermore, it cannot be repeated intraoperatively because of the increased risk of false positives. The newer imaging modalities focus on tissue oxygen tension (StO2) by mapping oxygen saturation indices. They utilize multispectral illumination to accurately quantify StO2 levels by distinguishing between oxyhemoglobin and deoxyhemoglobin without the need for fluorescent dyes or repeat intraoperative evaluations, thereby improving efficiency and accuracy.

Studies that have used StO2 to predict anastomotic leak after colo-rectal surgery in humans have utilized serosal oxygen tension, and these have established safety, usability, and reliability, along with exploration of the link with anastomotic leak. However, since the mucosa exhibits the first signs of hypoxia, it might be a better target for predicting postoperative anastomotic complications. Such a theory has been explored using the Food and Drug Administration (FDA) 510k approved device (FUJIFILM Eluxeo Vision system; K203717) among patients undergoing thoracic esophagectomy, in which the results followed the aforementioned hypothesis. However, there is no literature on such an imaging modality used for colon and/or rectal resections and anastomosis.

In this prospective observational study we aim to investigate the association between mucosal StO2 levels and the incidence of anastomotic complications, including stricture and leak in colo-rectal surgery. We hypothesize that lower StO2 will be associated with higher anastomotic complications (stricture and leak [grades A, B, or C], as determined by the surgeon).

Being tested
A novel endoscopic imaging system that displays real-time oxygen saturation levels
Keywords
anastomotic leak, colorectal, endoscopic, oxygen tension, oxygen saturation, mucosal, colon, rectum
Medical subject headings
Anastomotic Leak

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • A novel endoscopic imaging system that displays real-time oxygen saturation levelsDevice

    The imaging system in this study maps mucosal oxygen tension, where tissue first shows signs of hypoxia, rather than serosal oxygen tension, which has been the focus of previous studies

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Anastomotic complications

    leaks and strictures

    Measured: 30 days

Secondary outcomes (3)
  1. Surgical complications

    Surgical complications will be defined as any complication considered at least Grade I using the Clavien-Dindo classification system

    Measured: 30 days

  2. Surgical site infections

    Surgical site infections will be determined according to The Centers for Disease Control Surgical Site Infection Criteria and will include incision site and local infections at sites of organ manipulation.

    Measured: 30 days

  3. Respiratory infections

    A respiratory infection will be defined by a new or progressive infiltrate on chest radiography along with ≥2 of the following: WBC count >1.1 x 103/mm3 or < 4.5 x 103/mm3, purulent sputum, fever of >38°C or any new-onset signs of inflammation on auscultation.

    Measured: 30 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Mar 2026
  2. Study start16 Mar 2026
  3. Primary completionApr 2027 (estimated)
  4. Study completionApr 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
80 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07467980
Sponsor's protocol ID
250787
Other IDs
VUMC131557
Acronym
e-COMET
Status last verified
Jun 2026
First submitted
8 Mar 2026
Last updated
11 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
No: We will not share individual participant data (IPD) outside the study team due to privacy protections, consent limitations, and the risk of re-identification. Data will be stored securely and accessed only by authorized personnel. All results will be presented in aggregate form (summaries/tables) so that no individual can be identified.

Publications

  • Sherwani M, Ali D, Williams PJ, McChesney S, Ford MM, Hawkins AT, Muldoon R, Hopkins B, Geiger TM, Khan A. Prospective single-arm observational study evaluating a novel imaging device to assess anastomotic site mucosal oxygen tension and its association with anastomotic complications: study protocol. BMJ Open. 2026 Aug 25;16(8):e120491. doi: 10.1136/bmjopen-2026-120491.

    PubMed 42642079

Questions about this trial

What is this clinical trial studying?

An observational study of Anastomotic Leak Rectum and Anastomotic Leak Large Intestine, run by Vanderbilt University Medical Center at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 11 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Aimal Khan (+1 (615)343-4612, aimal.khan@vumc.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Anastomotic complications (time frame: 30 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07467980, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Jun 2026.

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