Electrosurgical Intervention Analysis: Comparing Procedure Patterns

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorUniversity Hospital Tuebingen

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

160 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University Hospital Tuebingen

Lead sponsor

Erbe Elektromedizin GmbH

Collaborator