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Ergonomics clinical trials

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NCT ID: NCT03339960 Recruiting - Ergonomics Clinical Trials

Ergonomics of Laparoscopy: Robotic Camera Controlled Versus Human Camera Controlled

Start date: June 23, 2017
Phase: N/A
Study type: Interventional

Minimal invasive surgery has acquired increased importance and the number of procedures performed is ever growing. Laparoscopic surgery has several distinct key benefits for patients over open surgery and therefore it is considered as standard treatment for most general surgery procedures. These benefits include faster recovery, shorter hospital stay, reduced post-operative pain and improved cosmetic results. However, laparoscopy has an increased burden to surgeons and many surgeons experience fatigue and physical discomforts due to laparoscopy. Robotic systems have been developed to improve the ergonomics (among other things), with good results. Many of the laparoscopy disadvantages have been overcome by robotic assisted surgery, such as increased range of motion, correction of the inverted instruments, and elimination of tremors.(4) Moreover, visualization of the operation is improved by personal camera control and stabilization of the image. The AutoLap system, a video analytic robotic camera holder, has been developed to hold the camera in a stable manner. It enables the surgeon to control the camera and eliminates the need for coordination and communication between surgeon and assistants. This study aims to evaluate the ergonomics of the surgeon and assistant during laparoscopy with the aid of the AutoLap system and compare it to standard laparoscopy. Also, it will be assessed whether the AutoLap can reduce physical and mental discomfort of both the surgeon and the assistant. Objective This multicenter randomized controlled trial aims to compare ergonomics of the OR nurse and the surgeon during standard laparoscopic procedures with laparoscopic procedures aided by a robotic camera holder, the AutoLap system. Study design Prospective, interventional, open, multicenter randomized controlled trial. The study will be conducted in Wilhemina Hospital Assen and in Meander Medical Center Amersfoort. Study population Adults ≥18 years who are scheduled for the following procedures: - Laparoscopic hiatal hernia repair / fundoplication - Laparoscopic right hemicolectomy - Laparoscopic sigmoid resection - Laparoscopic rectopexy - Laparoscopic low anterior resection - Laparoscopic splenectomy Inclusion criteria 1. Aged ≥ 18 years 2. Fit for standard laparoscopic general surgery Exclusion criteria 1. Contra-indications for laparoscopy 2. Obesity (BMI >35 Kg/m2) Intervention AutoLap group: In the AutoLap group, the camera will be held by a robotic arm. Posture of the surgeon and the assistant will be recorded during standardized predefined steps of the procedure. Control group: In the control group the camera will be held and maneuvered by a human assistant. The procedures will be performed according to the hospital and OR routine procedure. The surgical team will consist of 2 assistants and a surgeon. One of the assistants (OR-nurse, intern or resident) will hold the laparoscope and maneuver it. Posture of the surgeon and the assistant that maneuvers the laparoscope will be recorded during standardized predefined steps of the procedure. Main study parameters/endpoints: - RULA score, measured during predefined steps of the procedures. Secondary parameters/endpoints: - Questionnaires: Subjective Mental Effort Questionnaire (SMEQ), Local Experienced Discomfort (LED) scale (before and after the operation), NASA Task Load Index (NASA TLX).

NCT ID: NCT03096769 Completed - Ergonomics Clinical Trials

Ergonomics in Robotic Surgery

Start date: February 2, 2017
Phase: N/A
Study type: Interventional

This study is designed to answer if an ergonomist can configure a daVinci robot console to improve surgeon discomfort. Adjustments to the robot console will be surgeon specific as they are tailored to their individual body type. Measurements will be taken at the time of console configuration.

NCT ID: NCT01903577 Terminated - Ergonomics Clinical Trials

Comparative Ergonomic Analysis of Robotic Versus Laparoscopic Surgery

Start date: September 2012
Phase: N/A
Study type: Interventional

Robotic surgery holds the potential to overcome many of the ergonomic challenges posed by laparoscopic surgery. In this study, we propose to quantify this potential ergonomic benefit by measuring electromyography (EMG) and instrument motion analysis of subjects performing surgical tasks using robotic assistance versus standard laparoscopic instrumentation. Hypothesis: We hypothesize that surgeons will experience significant, measurable ergonomic advantages when performing tasks using robotic surgery when compared to conventional laparoscopic tools. Study design: Subjects for the study will include three groups of varying degrees of training - (1) novice laparoscopists/novice roboticists, (2) expert laparoscopists/novice roboticists, and (3) expert laparoscopsts/expert roboticists. Subjects will perform the following tasks (chosen based on their reliability and validity in previous studies). Each task will be performed with standard laparoscopic instrumentation and with the da Vinci Surgical System. - Inanimate (dry lab): Fundamentals of Laparoscopic (FLS) peg transfer, pattern cutting, intracorporeal suturing. - Animate (porcine lab): laparoscopic bowel resection and anastomosis, robotic bowel resection and anastomosis. - Human (clinical case): any laparoscopic or robotic procedure (preferably laparoscopic bowel resection and anastomosis, robotic bowel resection and anastomosis). Outcome measures: - Time to completion of tasks - EMG: peak amplitudes, % maximum voluntary contraction and frequency analysis - NASA Task Load Index scores - Subject-Reported Qualitative Data from surveys - Quality analysis of tasks (e.g., pattern cutting accuracy, % knots tied securely) for dry lab and animate lab tasks only) - Instrument motion analysis of tasks (for dry lab and animate lab tasks only)