Laser light may help surgeons spot risky bowel connections
NCT ID NCT07799740
First seen Sep 02, 2026 · Last updated Sep 03, 2026 · Updated 1 time
Summary
This trial tests whether a laser-based imaging device can help surgeons assess blood flow in the bowel during rectal cancer surgery. About 100 adults with rectal cancer will have the laser imaging performed alongside standard fluorescence imaging. The goal is to see if the laser tool is practical in the operating room and whether it might help surgeons choose where to cut, potentially reducing the chance of a serious complication called anastomotic leakage.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Laser speckle contrast imaging (PerfusiX-Imaging) compared with indocyanine green fluorescence imaging
- What this could lead to
- If it works, this imaging method could help surgeons choose safer cutting points during rectal cancer surgery, potentially lowering the risk of anastomotic leakage.
- What could go wrong
- This is an early feasibility study, so it may not prove that the imaging improves outcomes. The technique is new for laparoscopic use, and technical issues or surgeon acceptance could limit its usefulness.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥ 18 years * Rectal cancer * Surgical strategy either partial or total mesorectal excision * Able to provide informed consent Exclusion Criteria: \- Allergy to iodine
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Regional Hospital Gødstrup
Herning, Denmark
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Sygehus Lillebælt, Vejle Hospital
Vejle, Denmark
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Leveraging digital health solutions to collect Patient-Reported outcomes in rectal cancer
- Can a targeted drug conjugate outsmart advanced colorectal cancer?
- Can a platform trial match the right drug combo to each tumor?
- Dye-Guided surgery may spare healthy lymph nodes in esophageal cancer
- Can a counseling program restore intimacy after rectal cancer?