Evaluating ergonomic benefits of robot-assisted laparoscopic surgery for hysterectomies
Ergonomic Benefits from Robotically Assisted Laparoscopy for Hysterectomies and Other Selected Indications in Comparison to Conventional Laparoscopy - an Explorative Study
This study is testing if robot-assisted surgery for hysterectomies is easier on surgeons' bodies and minds compared to traditional surgery methods.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 4 (estimated) |
| Ages | 18 Years to 68 Years |
| Sex | All |
| Sponsor | University Hospital Tuebingen Academic / other |
| Locations | 1 site (Tübingen, Baden-Württemberg) |
| Trial ID | NCT06109753 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are trained surgeons aged 18 to 68 who are proficient in both robot-assisted and conventional laparoscopic surgeries.
Not a fit: Patients who are currently under the influence of analgesics or muscle relaxants, or those with acute diseases or muscle injuries, may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical techniques that reduce physical and mental strain on surgeons.
How similar studies have performed: Previous studies with similar designs have shown promising results, indicating that this approach is grounded in established research.
Eligibility criteria
Show full inclusion / exclusion criteria
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 this trial is running
Tübingen, Baden-Württemberg
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.