A Study to Evaluate the Safety and Effectiveness Transdermal Compress Device in Participants With Transfemoral Amputations

PHASE3RecruitingINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

June 11, 2024

Primary Completion Date

December 31, 2030

Study Completion Date

June 30, 2031

Conditions
Prosthesis and Implants
Interventions
DEVICE

Transdermal Compress Device

Study participants will undergo surgical implantation of the Transdermal Compress device on Study Day 1. Participants will be followed through the end of the study as they complete rehabilitation.

Trial Locations (9)

10065

RECRUITING

Memorial Sloan Kettering Cancer Center, New York

15232

RECRUITING

University of Pittsburgh Medical Center, Pittsburgh

19104

RECRUITING

Penn Medicine; University of Pennsylvania Health System, Philidelphia

20814

RECRUITING

Walter Reed Military Medical Center, Washington D.C.

21287

RECRUITING

The Johns Hopkins Hospital, Baltimore

43210

RECRUITING

The Ohio State University Wexner Medical Center, Columbus

60611

RECRUITING

Northwestern Memorial Hospital, Chicago

80045

RECRUITING

University of Colorado Anschutz Medical Campus, Aurora

95817

RECRUITING

UC Davis Medical Center, Sacramento

All Listed Sponsors
lead

Balmoral Medical company

INDUSTRY