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Ergonomic Benefits From Robotically Assisted Laparoscopy for Hysterectomies and Other Indications

Ergonomic Benefits From Robotically Assisted Laparoscopy for Hysterectomies and Other Indications

Not Recruiting
18-68 years
All
Phase N/A

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Overview

This is a prospective, single-center, observational clinical trial at the Department of Women's Health of the University Hospital Tübingen.

Description

Monocentric trial to evaluate differences in musculoskeletal and cognitive demands of robot-assisted laparoscopic surgery (RALS) vs. conventional laparoscopic surgery (CLS). Demographic and personal data are collected and pseudonymized. During surgery surface electromyography (EMG), electrocardiography (ECG), motion tracking data are collected and the surgery is documented by photos (1 photo/per second). Additionally, perceived physical discomfort (frequency and intensity) and mental load will be assessed within certain time intervals and at the very end of the surgery. The surgeon will not be disturbed in his actions and movement by the measurement equipment or applied procedures. Previous studies with similar designs can be seen as references in this context (549/2012BO1, 409/2013BO1, 262/2018BO1). After completing the surgery, the surgeon will rate difficulty of the surgery, work precision, eye strain and ergonomics during the surgery. Routine interventions like hysterectomies and other selected indications will be analyzed.

Eligibility

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

Study details
    Musculoskeletal Diseases or Conditions

NCT06109753

University Hospital Tuebingen

30 January 2026

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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