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.
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.
Study Type
OBSERVATIONAL
Enrollment
500
Patients are approached surgically with the Senhance Surgical System
St. Marien-Krankenhaus
Siegen, Germany
RECRUITINGAdverse Event
Any untoward sign symptom or disease
Time frame: Surgery to 30 days post op
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