At a glance
ClinicalIndex Comparison RecordN/ACompleted· 25 enrolled
Drug / intervention
Otto Bock C-Leg +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Comparative Outcomes Assessment of the C-Leg With a New Knee Prosthesis
In Brief
A clinical study evaluating Otto Bock C-Leg and Otto Bock Genium for Other and Unspecified Complications of Amputation Stump. Completed, enrolled 25 participants across 1 site.
Detailed Summary
The purpose of this study is to determine if transfemoral amputees of varied etiology will demonstrate increased function, safety and quality of life following accommodation with a new knee prosthesis as compared to their former C-Leg knee prosthesis.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsOtto Bock Healthcare, Florida High Tech Corridor Council
Timeline
N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
Enrollment StartJan 2011
First PostedNov 2011
Primary CompletionFeb 2013
TodayJul 2026
First PostedNov 17, 2011
Enrollment StartJan 1, 2011
Primary CompletionFeb 1, 2013
TodayJul 2, 2026
Enrollment to primary: 2.1 yearsPosted 14.6 years ago
Interventions
Otto Bock C-Legdevice
Amputees' preferred prosthetic knee.
Otto Bock Geniumdevice
Study knee.