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Robotics clinical trials

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NCT ID: NCT05071248 Completed - Patient Activation Clinical Trials

Evaluation of the Effect of Robot-assisted Early Mobilization - Project MobiStaR

MobiStaR
Start date: September 15, 2021
Phase: N/A
Study type: Interventional

Within the MobiStaR project the adaptation of procedures in an intensive care unit combined with the use of this robotic system will create the conditions to increase the mobilization rate of critically ill intensive care patients significantly, possibly thereby increasing the rehabilitation outcomes for these patients and developing a new standard of care for robot-assisted early mobilization. The intervention study will assess the organizational feasibility of robot-assisted early mobilization (starting in the first 72 hours after admission to the ICU), the behavior and experience of the mobilizing professionals and the effects on patient outcomes in terms of ventilation time, muscle mass (sonographic examination) and physical activity (measured by established scores such as Functional Status Score for ICU (FSS-ICU) and Medical Research Council (MRC) classification).

NCT ID: NCT04781101 Completed - Cerebral Palsy Clinical Trials

Can Robot-Assisted Gait Training In Addition To Conventional Rehabilitation Provide Better Outcomes In Children With Cerebral Palsy?

Start date: February 15, 2019
Phase: N/A
Study type: Interventional

A total of 26 patients who were diagnosed with CP [diplegic, with Gross Motor Function Classification System (GMFCS) level of 2-5] and who regularly participated in a rehabilitation programme were included in the study after obtaining approval from their parents. The patients were randomly assigned to two groups. Group 1 (n = 13) received conventional therapy (65 min, 2 days/week ×8) and group 2 (n = 13) received 25 minutes of robot-assisted gait training (RoboGait®) in addition to conventional therapy (40 min, 2 days/week ×8).

NCT ID: NCT04750265 Completed - Covid19 Clinical Trials

Robotic Assisted Early Mobilization in Ventilated ICU Patients With COVID-19

Start date: March 29, 2021
Phase: N/A
Study type: Interventional

Feasibility trial investigating the potential higher frequency of robotic assisted early mobilization in intubated COVID19 patients on the ICU.

NCT ID: NCT04721392 Completed - Healthy Clinical Trials

Mental Fatigue and Industrial Work Performance

Start date: March 8, 2021
Phase: N/A
Study type: Interventional

To investigate the effect of mental fatigue on industrial work performance, biomechanical determinants, (electro-)(psycho-) physiological measures and physical ergonomics. Additionally, the current project wants to evaluate whether or not the Laevo exoskeleton influences the aforementioned parameters when mental fatigue is acutely induced.

NCT ID: NCT04452695 Completed - COVID-19 Clinical Trials

Acceptability of Telehealth Triage Using Robotic Systems in COVID-19

Start date: March 10, 2020
Phase:
Study type: Observational

The overall objective of this investigation is to understand the patient response to a robotic platform used to facilitate telehealth triage in the emergency department during the COVID-19 pandemic. The COVID-19 pandemic has altered the manner in which emergency department triage is completed. Attempts at cohorting individuals with potential COVID-19 disease in order to prevent disease transmission to healthcare workers and minimize the use of personal protective equipment (PPE) have renewed interest in telemedical solutions as a method to triage and manage individuals with COVID-19. This investigation deploys a legged robotic platform to facilitate agile, highly mobile telemedicine to manage COVID-19 patients in the emergency department. The primary objective is to measure the patient response to interacting with these systems.

NCT ID: NCT04187209 Completed - Stroke Clinical Trials

Evaluation of the Use of the Atalante System in Patients Presenting a Non-traumatic Hemiplegia in Acute-subacute Phase (15 Days to 6 Months).

SPIRIT
Start date: September 11, 2019
Phase: N/A
Study type: Interventional

The SPIRIT study is interventional, national, prospective, open, bicentric each patient being his/her own control. It is conducted to assess the safety and performance of the Atalante exoskeleton system in patients presenting a non-traumatic acute-subacute hemiplegia. The primary endpoint is defined by the patient's ability to perform the 10 MWT with the Atalante system. The study will include 16 patients and takes place in two french rehabilitation centers.

NCT ID: NCT04110561 Completed - Clinical trials for Spinal Cord Injuries

Evaluation of Safety and Performance of the Atalante System With Patients With Lower Limb Paralysis

Start date: May 5, 2018
Phase: N/A
Study type: Interventional

The study is a prospective, open, bicentric and observational study. It is conducted to assess the safety and performance of the Atalante exoskeleton system with patients with lower limb paralysis. The principal objective is to assess the performance of the Atalante system in performing ambulatory functions with motor complete SCI patients characterized by the success rate in performing a 10mWT at the last session of training with the Atalante system.

NCT ID: NCT03659318 Completed - Arthritis Clinical Trials

Robotic-Assisted Versus Conventional Total Knee Arthroplasty(TKA)

Start date: January 2002
Phase: Phase 4
Study type: Interventional

Robotic-assisted total knee arthroplasty (TKA) was introduced to attempt to enhance the precision of bone preparation, component alignment and ultimately improve clinical results and survivorship of TKA. Although several published data suggest that bone preparation, and knee component alignment were improved by using robotic assistance, there is no high-quality evidence from randomized trials at long-term of which investigators are aware evaluating whether the improved bone preparation and knee component alignment improved clinical function or longevity of the TKA.

NCT ID: NCT03183856 Completed - Clinical trials for Arthroplasty, Replacement, Knee

Comparison of Ambulatory and Functional Improvement by Morning Walk

Start date: September 15, 2017
Phase: N/A
Study type: Interventional

The aim of this study is to determine the clinical efficacy and feasability of gait rehabilitation robot through approving functional improvement by an end-effector typed gait robot in patients underwent total knee arthroplasty.

NCT ID: NCT01705821 Completed - Robotics Clinical Trials

Forces During Skull Base Surgery

Start date: October 2012
Phase: N/A
Study type: Observational

This study is designed to measure forces applied using standard surgical instruments at the skull base during resection of skull base lesions. This data will be useful for optimizing an active canula robot for assisting in skull base surgery. We hypothesize that through measurement of forces generated during routine endoscopic skull base surgery we will be able to optimize the canulas of an active canula robot for skull base surgery.