Analyzing Electrosurgical Procedure Patterns

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to verify the hypothesis that different electrosurgical interventions create unique data patterns, akin to digital fingerprints. By utilizing the Erbe ESU VIO 3 and the ECB Data Transmitter, the study will record high-accuracy electrical data during various surgical procedures. The collected data will be stored in the Azure Cloud and will not contain any patient information, focusing solely on enhancing clinical workflows and training opportunities for surgical teams.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age ≥ 18 years
* Written informed consent
* Patients undergoing one of the following surgeries:

  * Supra cervical hysterectomy
  * Total hysterectomy
  * Breast conserving surgeries: B-plastic + periareolar mastopexy
  * Breast conserving surgeries: segmental resection

Exclusion Criteria:

* 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

Where it's running

• University Hospital Tuebingen
  Tübingen, Germany Recruiting

Study contacts

• Principal investigator: Bernhard Krämer, Prof. Dr. — University Hospital Tuebingen
• Study coordinator: Bernhard Krämer, Prof. Dr.
• Email: Bernhard.kraemer@med.uni-tuebingen.de
• Phone: +497071-2982211

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.