An Investigation Into a New Manufacture Technique of Trans-femoral Sockets
Completed · Not applicable
Conditions studied: Amputation
In brief
The investigation will be of a single group prospective pre/post design with follow up at 6 weeks (6WFU) and 6 months (6MFU); comparing to outcomes at baseline (BL). Device(s) being tested: Interchangeably: Direct Socket TF; DS-TF; DS Trans-femoral. The DS-TF is a trans-femoral (TF) set-up of the currently marketed trans-tibial version. It is not marketed in the USA and has not been registered with the FDA. The comparator is the current socket the subject is using when enrolled in the study. Subjects recruited: Minimum 50 Inclusion criteria: 50Kg\< body weight \< 160Kg Cognitive ability to understand all instructions and questionnaires in the study; Patients who have undergone a transfemoral amputation \> 1 year post amputation Older than 18 years Willing and able to participate in the study and follow the protocol Circular dimension of 40-65 cm at the crotch Residual limb length at least 20 cm from ischium to distal end Currently using a prosthetic liner Locking users that can successfully be fitted with Iceross® Transfemoral Locking, OR Seal-In users that can successfully be fitted with either Iceross Seal-In® X5 TF or Iceross Transfemoral Seal-In® Exclusion criteria: 50Kg\> body weight \> 160Kg Users with cognitive impairment Patients who have undergone a transfemoral amputation \<1 year post amputation Younger than 18 years Not a prosthetic ambulator, uses only the prosthesis for cosmetic reasons Circular dimension of less than 40 cm or greater than 65 cm at the crotch Residual limb length less than 20 cm from ischium to distal end Currently not using a prosthetic liner
Key facts
- Study ID
- NCT04312724
- Run by
- Össur Iceland ehf
- People needed
- 47
- Starts
- 2018-04-30
- Expected to finish
- 2020-07-01
- Last updated by the study team
- 2020-11-20
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Cognitive ability to understand all instructions and questionnaires in the study.
- Patients who have undergone a trans-femoral amputation > 1 year post amputation.
- Willing and able to participate in the study and follow the protocol.
- Circular dimension of 40-65 cm at the crotch.
- Residual limb length at least 20 cm from ischium to distal end.
You may not qualify if…
- 50Kg > body weight > 160Kg
- Users with cognitive impairment
- Not a prosthetic ambulator, uses only the prosthesis for cosmetic reasons
Where it is running
- Alabama Artificial Limb Specialists — Mobile, Alabama, United States
- Alabama Artificial Limb Specialists — Montgomery, Alabama, United States
- Alabama Artificial Limb Specialists — Opelika, Alabama, United States
- Van Der Watt Prosthetics & Orthotics — Greenwood, Arkansas, United States
- Tillges Certified Orthotic Prosthetic Inc — Maplewood, Minnesota, United States
- Sampson's Prosthetics Lab — Albany, New York, United States
- Sampson's Prosthetics Lab — Schenectady, New York, United States
- Eastside Orthotics and Prosthetics — Portland, Oregon, United States
- Union Orthotics & Prosthetics Co — Cranberry Township, Pennsylvania, United States
- Union Orthotics & Prosthetics Co — East Rochester, Pennsylvania, United States
- Union Orthotics & Prosthetics Co — Greensburg, Pennsylvania, United States
- Union Orthotics & Prosthetics Co — Pittsburgh, Pennsylvania, United States
- Union Orthotics & Prosthetics Co — Pittsburgh, Pennsylvania, United States
- Victory Orthotics and Prosthetics Inc. — Johnson City, Tennessee, United States
- Victory Orthotics and Prosthetics Inc. — Kingsport, Tennessee, United States
- Victory Orthotics and Prosthetics Inc. — Knoxville, Tennessee, United States
- Virginia Prosthetics and Orthotics — Roanoke, Virginia, United States
Full record on ClinicalTrials.gov
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