Evaluating ergonomic benefits of robot-assisted laparoscopic surgery for hysterectomies

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 clinical trial aims to assess the differences in musculoskeletal and cognitive demands between robot-assisted laparoscopic surgery (RALS) and conventional laparoscopic surgery (CLS). Conducted at the University Hospital Tübingen, the study collects demographic data and utilizes surface electromyography (EMG), electrocardiography (ECG), and motion tracking during surgeries. Surgeons will also report on their perceived physical discomfort and mental load at various intervals throughout the procedure. The goal is to understand how these two surgical approaches impact surgeon ergonomics and overall performance.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age between 18 and 68 years
* surgeons that are able to work in full shift
* trained surgeons in RALS and CLS
* written informed consent

Exclusion Criteria:

* persons influenced by analgesics or muscle relaxants
* persons not able to perform their common work for any reason
* persons with acute diseases
* muscle injury

Where it's running

• University Women's Hospital
  Tübingen, Baden-Württemberg, Germany Recruiting

Study contacts

• Principal investigator: Benjamin Steinhilber, PD Dr. — Institute of Occupational and Social Medicine and Health Services Research
• Study coordinator: Bernhard Krämer, Prof. Dr.
• Email: bernhard.kraemer@med.uni-tuebingen.de
• Phone: : +49 7071 29 82211

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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.