The TransEnterix European Patient Registry

An open label observational registry trial in which participating centers enroll subjects who had or will have a laparoscopically assisted surgery using the Senhance Surgical System.

Why the study stopped: Terminated due to a business decision by the acquiring company to discontinue the marketed product. The post-market surveillance registry was no longer feasible. Not related to safety concerns.

Terminated

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Key information

Conditions

Surgery

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

St. Marien-Krankenhaus

Siegen, 57072, Germany

About this study

This is a prospective multi-center registry in which sites may also choose to retrospectively enroll subjects meeting the inclusion criteria, but whom have already been treated using the Senhance system. The data collection includes baseline patient characteristics, surgical details, and adverse events. Patient follow-up time point is open to the clinical practice of each center and only adverse events are tracked post discharge.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

patients 18-80 years old
Signed the informed consent
life expectancy 12 months or more

Exclusion criteria

Treatment and study plan

surgery

Device

Patients are approached surgically with the Senhance Surgical System

Primary outcomes

Adverse Event

Time frame: Surgery to 30 days post op

Any untoward sign symptom or disease

Sponsors and collaborators

Lead sponsor

Asensus Surgical

Industry

Collaborators

RQM+

Registry information

Official study title

The TransEnterix European Patient Registry for Robotic Assisted Laparoscopic Procedures in Urology, Abdominal Surgery, Thoracic and Gynecologic Surgery

Acronym: TRUST

Important dates

Study start: 2017
Primary completion: 2026
Study completion: 2026
First posted: Dec 28, 2017
Registry last updated: Aug 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Terminated