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