The purpose of this study is to evaluate the safety and effectiveness of the Transdermal Compress device in participants with Transfemoral Amputations.
Prosthesis and Implants
The purpose of this study is to evaluate the safety and effectiveness of the Transdermal Compress device in participants with Transfemoral Amputations.
A Study to Evaluate the Safety and Effectiveness Transdermal Compress Device in Participants with Transfemoral Amputations
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UC Davis Medical Center, Sacramento, California, United States, 95817
University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States, 80045
Walter Reed Military Medical Center, Washington, District of Columbia, United States, 20814
Northwestern Memorial Hospital, Chicago, Illinois, United States, 60611
The Johns Hopkins Hospital, Baltimore, Maryland, United States, 21287
Memorial Sloan Kettering Cancer Center, New York, New York, United States, 10065
The Ohio State University Wexner Medical Center, Columbus, Ohio, United States, 43210
Penn Medicine; University of Pennsylvania Health System, Philidelphia, Pennsylvania, United States, 19104
University of Pittsburgh Medical Center, Pittsburg, Pennsylvania, United States, 15232
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
For general information about clinical research, read Learn About Studies.
18 Years to 65 Years
ALL
No
Balmoral Medical company,
David Recker, M.D., STUDY_DIRECTOR, Balmoral
2031-06