Actively Recruiting
Electrical Fingerprint: Comparison of Characteristic Patterns of Different Surgical Interventions Based on Electrosurgical Unit Data
Led by University Hospital Tuebingen · Updated on 2026-01-26
160
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University Hospital Tuebingen
Lead Sponsor
E
Erbe Elektromedizin GmbH
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating electrical data patterns generated during different types of electrosurgical procedures to identify unique "digital fingerprints" for each intervention. This study aims to differentiate surgical workflows by analyzing high-accuracy electrical measurement data collected from the Erbe ESU VIO 3 device, with the goal of enhancing clinical training and procedure understanding. The study is observational and does not assess device performance or safety but collects and assigns electrical data only. During surgeries such as supra cervical hysterectomy, total hysterectomy, and breast-conserving surgeries including B-plastic with periareolar mastopexy or segmental resection, the VIO 3 device will be connected to a data transmitter that records electrical signals. These data are forwarded via network connections and stored securely in the cloud without patient information. The study also includes data from other procedures categorized as "unknown" types to build a comprehensive database. Participants will undergo one of the specified surgeries, during which electrical data will be collected. Researchers will analyze these data during and after surgery over a 12-month period to identify characteristic patterns. No patient information is stored with the electrical data, and no changes to usual surgical care occur. This study is conducted at a single center and aims to improve future training and self-reflection for surgical users based on the collected data patterns.
CONDITIONS
Brief Title
Electrosurgical Intervention Analysis: Comparing Procedure Patterns
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 2 18 years or older
- Written informed consent
- Patients undergoing one of the following surgeries: supra cervical hysterectomy, total hysterectomy, breast conserving surgeries including B-plastic with periareolar mastopexy, or segmental resection
You will not qualify if you...
- Expected lack of patient compliance or inability to understand the study purpose
- Lack of patient consent
- Surgery performed under local anesthesia
- Robot-assisted surgery planned or performed
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit
Duration - Day of surgery
Participants undergo one of the specified surgical procedures while electrosurgical data is recorded during the operation.
1 surgical procedure visit
Duration - Up to 12 months after surgery
Participants are observed as electrosurgical data from their procedure is collected and analyzed over time to identify unique procedure patterns.
Data collection via device during routine care; no additional visits required
Trial Site Locations
Total: 1 location
1
University Hospital Tuebingen
Tübingen, Germany, 72076
Actively Recruiting
Research Team
B
Bernhard Krämer, Prof. Dr.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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