A tiny sensor could watch over reconstructed tissue
NCT ID NCT07786610
First seen Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time
Summary
This observational study tests a new sensor that measures oxygen levels in tissue flaps during reconstructive surgery. The sensor is placed in the flap and tracks oxygen saturation continuously, comparing it to blood samples and key surgical events. The goal is to see if this technology can reliably detect changes in blood flow, which could help surgeons prevent complications. The study involves 30 adults undergoing flap reconstruction.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- SpectroCor Monitoring System (a spectroscopic sensor that measures tissue oxygen saturation)
- What this could lead to
- If successful, this could lead to a reliable way to monitor tissue flaps during surgery, potentially reducing the risk of flap failure and improving surgical outcomes.
- What could go wrong
- This is a small observational study, so it may not prove the sensor's effectiveness. The sensor is experimental and could have technical issues or cause discomfort.
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.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 2031
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients scheduled for plastic surgical reconstructive flap operation in the Helsinki University Central Hospital.
- Ages
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18 to 90 years
- 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: * Adults, age of 18 - 90 years * Scheduled for plastic surgical reconstructive flap operation * Ability and willingness to provide informed consent. Exclusion Criteria: * Unable to provide signed informed consent * Considered a vulnerable person according to the Finnish Medical Research Act (488/1999), Chapter 2, Sections 7, 9, and 10, including retarded persons, pregnant women, nursing mothers, prisoners, and forensic patients.
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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 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.
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