Powered Prosthetics for Knee Amputations
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores how powered prosthetics can improve walking for individuals with above-knee amputations. Researchers aim to determine if adding power to the knee, the ankle, or both can enhance walking ease and efficiency. Participants will test various prosthetic combinations, including the SRALab Hybrid Knee and SRALab Polycentric Powered Ankle, and receive training to identify the most effective option. Ideal candidates have a transfemoral amputation (above the knee), have used a prosthetic leg for at least six months, and can walk 50 meters unaided.
As an unphased trial, this study allows participants to contribute to innovative research that could enhance mobility for many.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications. Please consult with the study team or your doctor for guidance.
What prior data suggests that these powered prosthetics are safe for transfemoral amputees?
Research has shown that powered prosthetic devices, such as the SRALab Hybrid Knee and SRALab Polycentric Powered Ankle, are generally easy for users to handle. In studies where participants tried these devices, researchers found no major safety issues. For instance, one study with a 70-year-old man who had a leg amputation demonstrated that he could use these devices effectively after some training. This suggests they can be safe and manageable with proper guidance.
These devices are part of research aimed at improving walking for people with above-knee amputations. They are not yet approved for widespread use, so researchers continue to closely monitor safety. While some minor discomfort or adjustment issues might occur, major problems are not commonly reported.12345Why are researchers excited about this trial?
Researchers are excited about the SRALab Hybrid Knee and SRALab Polycentric Powered Ankle because these devices offer dynamic, powered support that closely mimics natural leg movement, unlike current prosthetic options like the Ottobock C-Leg, which primarily offer passive support. The Hybrid Knee's advanced microprocessor technology adjusts in real-time to the user's movement, providing smoother transitions and more natural walking patterns. Meanwhile, the Polycentric Powered Ankle enhances stability and adaptability across various terrains, potentially improving balance and reducing the effort required for walking. These innovations aim to empower users with greater mobility and independence, sparking hope for a significant leap in quality of life for those with knee amputations.
What evidence suggests that these prosthetic devices are effective for improving ambulation in knee amputees?
This trial will evaluate the effectiveness of powered prosthetics, such as the SRALab Hybrid Knee and SRALab Polycentric Powered Ankle, for individuals with knee amputations. Research has shown that these powered prosthetics can greatly improve walking compared to non-powered prosthetics. Participants will be assigned to different arms, receiving either the SRALab devices or other prosthetic combinations like the Ottobock Cleg4 and foot. These devices add strength to the missing joints, helping users walk more naturally and efficiently. Early results suggest that powering both the knee and ankle might further boost walking ability. With focused training on these powered devices, users may experience even greater improvements, leading to better mobility in everyday life.13567
Are You a Good Fit for This Trial?
This trial is for K2-level transfemoral amputees, meaning individuals who have had an above-knee amputation and can walk with a cane or crutches. The study aims to understand the impact of powered prosthetic knees and ankles on their walking ability.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Baseline Assessment
Baseline data collection with Ottobock Cleg 4/Ottobock foot or clinically prescribed microprocessor knee unit/foot
Condition A: CLeg + Polycentric Ankle
Participants are fit with the CLeg + Polycentric Ankle and undergo device tuning and functional outcome assessments
Condition B: SRALab Hybrid Knee + Passive Ankle
Participants switch to SRALab Hybrid Knee + Passive Ankle and repeat the protocol for device tuning and assessments
Intensive Training
Participants receive intensive clinical training with the SRALab Hybrid Knee + Polycentric Ankle
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- SRALab Hybrid Knee and SRALab Polycentric Powered Ankle
Trial Overview
The study compares different combinations of prosthetic limbs: a passive microprocessor knee (Ottobock CLeg4) with either an Ottobock foot or polycentric ankle, and a powered knee (SRALAB Hybrid Knee) with either a passive or polycentric powered ankle.
How Is the Trial Designed?
3
Treatment groups
Experimental Treatment
Active Control
During this arm, participants will receive intensive clinical training with the SRALAB Hybrid knee + Polycentric Ankle twice per week over 8 weeks, lasting 2-3 hours. Training will include patient-driven therapy to achieve participants' individual therapy goals, functional mobility and community skills. At the end of the 8-week training period, subjects will complete the same set of functional outcome measures, biomechanical and metabolic assessments in previous arms. To complete this arm, participants will again complete training and outcome measures with the Ottobock Cleg4/Ottobock or their clinically prescribed microprocessor knee unit/foot over 3 visits.
For this arm, transfemoral amputees will participate in an AB/BA randomized crossover study. Before each arm of the cross-over, baseline data will be taken with the Ottobock Cleg 4/Ottobock foot or their clinically prescribed microprocessor knee unit/foot. Condition A is CLeg + Polycentric Ankle Condition B is SRALab Hybrid knee + Passive Ankle Subjects will participate in 2 sessions over 2 weeks, each lasting 2-3 hours to have the device tuned for the specific condition (A or B). On the third week, they will participate in 2 visits to complete functional outcome measures, biomechanical and metabolic assessments. They will then switch conditions, and repeat the protocol for the second condition. There will not be a washout period between conditions, but subjects will complete outcome measures with the Ottobock Cleg 4/Ottobock foot or their clinically prescribed microprocessor knee unit/foot prior to each arm of the crossover to obtain baseline data.
Participant is fit with the commercially available device (Ottobock Cleg 4/Ottobock foot), they will receive standard of care clinical training for 3-4 sessions over 4 weeks, plus 1 session for outcome assessments. Participant is then fit with the SRALAB Hybrid knee and SRALAB Polycentric Ankle prosthesis, they again will receive clinical training for 3-4 sessions over 4 weeks, plus 1 session for outcome assessments.
SRALab Hybrid Knee and SRALab Polycentric Powered Ankle is already approved in United States for the following indications:
- Transfemoral amputation for K2 level ambulators
Find a Clinic Near You
Who Is Running the Clinical Trial?
Shirley Ryan AbilityLab
Lead Sponsor
Published Research Related to This Trial
Citations
Powered Prosthetics for Knee Amputations
What data supports the effectiveness of the treatment SRALab Hybrid Knee and SRALab Polycentric Powered Ankle for knee amputations? Research on similar ...
2.
trial.medpath.com
trial.medpath.com/clinical-trial/11b552b93c2bfbdb/nct06433648-powered-componentry-k2-transfemoral-amputee-gaitUnderstanding How Powered Componentry Impacts K2-Level ...
The goal of this study is to understand how providing power at the knee or ankle individually, or providing power at both the knee and ankle, ...
Amputation Clinical Trials - Policy Lab
A listing of 39 Amputation clinical trials actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
Evaluation of a Lightweight Powered Leg
We have designed a lightweight powered leg with innovative knee and ankle designs that significantly reduce weight and noise while providing necessary power ...
5.
frontiersin.org
frontiersin.org/journals/rehabilitation-sciences/articles/10.3389/fresc.2023.1203545/fullPowered knee and ankle prosthesis use with a K2 level ...
Powered prosthetic knees and ankles have the capability of restoring power to the missing joints and potential to provide increased functional mobility to ...
Powered knee and ankle prosthesis use with a K2 level ...
We trained a 70 year old male participant with a unilateral transfemoral amputation to use a powered knee and powered ankle prosthesis.
7.
sralab.org
sralab.org/clinical-trials/limb-loss-impairment/intuitive-control-hybrid-prosthetic-leg-during-ambulationIntuitive Control of a Hybrid Prosthetic Leg During Ambulation
The objective of this research is to determine the clinical benefits of an innovative and lightweight powered leg controlled using our intent recognition ...
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