About this trial
The purpose of this prospective, single center study is to verify the hypothesis that each type of intervention creates a specific data pattern like a digital "fingerprint". This fingerprint offers the possibility to identify specific workflows of surgical procedures but also to differentiate between them, what can be used for training purposes. The following clinical study is not covered by the MDR regulation since we do not investigate performance or safety of a device but collect and assign electrical data only.
Eligibility criteria
Qualifiers
Age ≥ 18 years
Written informed consent
Supra cervical hysterectomy
Total hysterectomy
Disqualifiers
Expected lack of patient compliance or inability of the patient to understand the purpose of the clinical trial
Lack of patient consent
Surgery under local anaesthesia
Robot-Assisted Surgery
Trial design
Treatments tested in this trial
- Procedure type
Treatment groups
Sponsors and collaborators
University Hospital Tuebingen
Lead sponsor
Erbe Elektromedizin GmbH
Collaborator