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Amputation, Traumatic clinical trials

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NCT ID: NCT04069793 Active, not recruiting - Amputation Clinical Trials

Functional Importance of a Powered Multifunction Wrist Protocol

Start date: January 18, 2018
Phase: N/A
Study type: Interventional

The focus of this study is to conduct a clinical study in individuals with transradial amputations to compare function using a 1-DOF or 2-DOF wrist. All prostheses will be attached to a single DOF Otto Bock hand and controlled using a pattern recognition system equivalent to the Coapt system. This study will enable the investigator to quantify the relative functional value of powered wrist flexion during both in-laboratory testing and home use. In addition, the investigators will address the effectiveness of different hand-wrist combinations to enhance patient-centered clinical decision making.

NCT ID: NCT04057989 Completed - Analgesia Clinical Trials

Retrospective Evaluation of Ketamine Effectiveness for the Treatment of Acute Battlefield Related Pain

Start date: August 2014
Phase:
Study type: Observational

Using a retrospective review of records, we will conduct a multivariate analysis to examine the relationship between exposure to ketamine, as an analgesic agent in combat related trauma care, the use of additional opioid pain medications, and patient reported pain levels.

NCT ID: NCT04038580 Active, not recruiting - Amputation Clinical Trials

A Comparative Assessment of Transfemoral Prosthetic Sockets

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

The objective of the proposed work is to enhance understanding of the potential benefits of adjustable sockets and inform clinical decision making.

NCT ID: NCT03968835 Withdrawn - Clinical trials for Amputation, Traumatic

A Comparison of the Outcomes of Distal Fingertip Amputations Treated With Either Artificial (Xeroform) or Biological Dressings

Start date: December 24, 2018
Phase:
Study type: Observational

This is a prospective study looking to evaluate whether the treatment outcomes for patients who sustain a distal fingertip amputation are improved or no different when using biological dressings versus artificial dressings.

NCT ID: NCT03924310 Completed - Clinical trials for Amputation; Traumatic, Hand

Sensor Glove and Non-Invasive Vibrotactile Feedback Insole to Improve Hand Prostheses Functions and Embodiment

FeetBack
Start date: August 9, 2021
Phase: N/A
Study type: Interventional

State-of-the-art myoelectric prostheses provide upper limb amputees with a remarkable variety of grip patterns but lack proper feedback from touch sensation. This restriction limits the controllability of multi-articulated robotic hands, resulting in the rejection of the device in many cases. Amputees have often reminiscing sensations in the stump, i.e. by touching certain regions, it feels as if no longer existing fingers were touched. These regions form a phantom map and show promising results for touch feedback. However, not every amputee has one and the socket of a prosthesis offers limited space for additional devices. Thus, the investigators developed a feedback display which is worn in the shoe instead of the prosthesis itself. The investigators want to assess the viability of vibrotactile feedback stimulus on the foot as a substitution for pressure on the fingers of an artificial hand in a clinical study. The efforts are based on the hypothesis that a hand prosthesis with tactile feedback has better performance in manipulating fragile and heavy objects, compared with a standard commercial hand prosthesis without tactile feedback.

NCT ID: NCT03876405 Completed - Prosthesis User Clinical Trials

Evaluation of a Non-invasive Sensory Feedback System in Hand Prostheses

Start date: April 1, 2015
Phase: N/A
Study type: Interventional

Implication and evaluation of a non-invasive sensory feedback system in hand prostheses in everyday life.

NCT ID: NCT03505983 Active, not recruiting - Prosthesis User Clinical Trials

Criteria for Advanced Prosthetic Foot Prescription

Start date: August 1, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to develop criteria for prosthetic foot prescription for Veterans and Service Members with transtibial limb loss. The objectives are to: 1) Determine the appropriate functional outcome tests and measures to support the prescription of a type of Energy Storing and Returning (ESR) non-articulating, articulating or active plantarflexion prosthetic ankle-foot for a Veteran or Service Member with transtibial limb loss. 2) Correlate patient goals and subjective measures with objective data to determine the appropriate prosthetic ankle-foot category that will facilitate the greatest overall function to the user. 3) Develop criteria for the appropriate prescription of non-articulating ESR, articulating ESR, and active plantar flexion ESR ankle-foot units.

NCT ID: NCT03498872 Completed - Prosthesis User Clinical Trials

Strategic Research Program 17 (VUB Funding)

Start date: October 1, 2016
Phase: N/A
Study type: Interventional

Objectives: The main objectives are to determine neural dynamics during gait using electro-encephalography as well as brain sources and to investigate the attentional demand during walking in able-bodied individuals, and individuals with an amputation. Materials & Methods: 6 able-bodied individuals conducted one experimental trial, and 6 unilateral transtibial and 6 unilateral transfemoral amputees performed 2 experimental trials; the first with the current and the second with a novel powered transtibial prosthesis, i.e. the Ankle Mimicking Prosthetic foot 4.0. Each experimental trial comprised 2 walking tasks; 6 and 2min treadmill walking at normal speed interspersed by 5min of rest. During 6min walking the sustained attention to response (go-no go) task, with measures reaction time and accuracy, was performed. Electro-encephalographic (EEG) data were gathered when subjects walked 2min. Motor-related cortical potentials and brain activity during gait are extracted using EEG.

NCT ID: NCT03412656 Completed - Clinical trials for Amputation, Traumatic

Assessing Force Feedback With the SoftHand Pro

CUFF
Start date: October 17, 2017
Phase: N/A
Study type: Interventional

The trial is designed to test the effectiveness of a force-feedback cuff in combination with a myoelectric prosthesis in conveying information on grasp strength to the user, as well as the user's preference regarding the feature.

NCT ID: NCT03400345 Recruiting - Hand Injuries Clinical Trials

Human Upper Extremity Allotransplantation: F/U Protocol

Start date: July 25, 2017
Phase:
Study type: Observational

Upper extremity allotransplantation is a new procedure which is becoming more common in the United States. Ongoing data collection for research purposes is vital to the long-term assessment as to the safety of the procedure and accompanying immunosuppression protocol, as well as quantifying patient outcomes and changes in quality of life. For these reasons, The Johns Hopkins Hand/Arm Transplantation Team is interested in enrolling transplanted patients in a follow-up protocol to continue collecting informative data to further the field of vascularized composite allotransplantation.