New device could make hysterectomy safer and faster
NCT ID NCT07226375
First seen Nov 10, 2025 · Last updated Jun 22, 2026 · Updated 31 times
Summary
This study compares a new endoscopic tissue cutting device to a traditional scalpel for removing large uteri (500 grams or more) after laparoscopic hysterectomy. The device is designed to cut and remove tissue through small incisions more quickly and safely, reducing the risk of spreading potentially cancerous cells. Researchers will measure how long it takes to remove the uterus and check for complications, as well as effects on sexual function.
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This is a summary of
the original study
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Izmir Bakircay University
RECRUITINGIzmir, 35665, Turkey (Türkiye)
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact
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 laparoscopic hysterectomy faster and safer by reducing the risk of tissue spreading and shortening surgery time.
What could go wrong
This is a small, early-stage trial with only 84 participants, so results may not apply to all patients. The device is new and its long-term safety and effectiveness are not yet proven.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.