New device aims to make hysterectomy tissue removal faster and safer
NCT ID NCT07226375
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tests a new medical device designed to cut and remove large tissue (like the uterus) through small incisions after laparoscopic hysterectomy. It compares the device to the traditional cold scalpel method in 84 women whose uterus weighs 500 grams or more. The main goal is to see if the device shortens removal time and reduces complications.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Endoscopic tissue cutting and abdominal extraction device
- What this could lead to
- If successful, this device could make tissue removal after laparoscopic hysterectomy faster and safer, reducing risks like cancer cell spread.
- What could go wrong
- This is a small, early-stage trial (84 people) comparing a new device to a standard scalpel. The device may not prove faster or safer, and unexpected complications could arise.
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 84 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2025
- Expected to finish
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Dec 2026
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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35 to 65 years
- Sex
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Female participants only
- 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: * Planned laparoscopic hysterectomy * Estimated uterine weight of 500 g or more Exclusion Criteria: * Sexual inactivity
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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
1 site. 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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Izmir Bakircay University
RECRUITINGIzmir, 35665, Turkey (Türkiye)
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