European registry launches to monitor robotic surgery safety

NCT ID NCT03385109

First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time

Summary

This observational registry is following 500 patients aged 18–80 who undergo robotic-assisted laparoscopic surgery using the Senhance Surgical System. The goal is to track any adverse events and gather real-world safety data across urology, abdominal, thoracic, and gynecologic procedures. No new treatment is being tested; instead, the registry collects information to better understand the risks and outcomes of this robotic surgical device.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

Senhance Surgical System (robotic surgical device)

What this could lead to

If successful, this registry will provide real-world safety data on robotic-assisted laparoscopic surgeries, potentially guiding future surgical practices.

What could go wrong

This is an observational registry, not a controlled trial, so it cannot prove cause and effect. Results may be influenced by differences in patient selection or surgical techniques across centers.

Disclaimer Read more

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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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • St. Marien-Krankenhaus

    RECRUITING

    Siegen, 57072, Germany

    Contact

    Contact Phone: •••-•••-•••• Email: •••••@•••••