Can a minimally invasive technique make limb perfusion safer?
NCT ID NCT03376126
First seen Aug 19, 2026 · Last updated Aug 20, 2026 · Updated 1 time
Summary
This trial is testing whether a minimally invasive version of isolated limb perfusion is feasible. Isolated limb perfusion is a procedure that delivers high-dose chemotherapy directly to a limb affected by cancer, but the standard approach requires a large incision. The study will enroll 15 adults scheduled for this treatment and measure how often the minimally invasive approach must be converted to open surgery, as well as how well patients respond and any complications. The goal is to see if this less invasive method can be a viable option.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Minimally-invasive isolated limb perfusion (a surgical technique to deliver chemotherapy directly to a limb)
- What this could lead to
- If successful, this could make isolated limb perfusion less invasive, potentially reducing recovery time and complications for patients with tumors in a limb.
- What could go wrong
- This is a small feasibility study, so it may not prove the technique works better than the standard approach. There is also a risk of complications or the need to convert to open surgery during the procedure.
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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15 people
The number who actually took part.
- Started
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Jun 2016
- Finished
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Jun 2026
- Lead sponsor
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A government agency
The lead sponsor is a government body.
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 isolated limb perfusion.
- 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: 1. The patient scheduled for treatment with isolated hyperthermic perfusion 2. Age over 18 years. 3. Signed informed consent Exclusion Criteria: 1. Re-perfusion 2. Lymph node metastases 3. Severe atherosclerosis
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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.
Contacts and locations
Locations
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Sahlgrenska University Hospital
Gothenburg, 413 45, Sweden