Hysterectomy Clinical Trials

Clinical trials related to Hysterectomy Procedure

Electrical Fingerprint: Comparison of Characteristic Patterns of Different Surgical Interventions Based on Electrosurgical Unit Data

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

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
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Germany
University Hospital Tuebingen
RECRUITING
Tübingen
Contact Information
Primary
Bernhard Krämer, Prof. Dr.
Bernhard.kraemer@med.uni-tuebingen.de
+497071-2982211
Time Frame
Start Date: 2024-02-21
Estimated Completion Date: 2026-06
Participants
Target number of participants: 160
Treatments
Procedure type
Procedures:~* Supra cervical hysterectomy (+/- salpingectomy)~* Total hysterectomy~* Breast conserving surgeries: b-plastic + periareolar mastopexy (+/- Sentinel lymphonodectomy, SLNE)~* Breast conserving surgeries: segmental resection (+/- SLNE)~Data will be collected among patients who undergo surgery at the Department of Women's Health independently of this study.
Unknown
Related Therapeutic Areas
Sponsors
Leads: University Hospital Tuebingen
Collaborators: Erbe Elektromedizin GmbH

This content was sourced from clinicaltrials.gov