At a glance
ClinicalIndex Comparison RecordN/ACompleted· 52 enrolled
Drug / intervention
nSTRIDE Autologous Protein Solution (APS) Kitdevice
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.
A Prospective Study of a Single Intra-Articular Injection of Autologous Protein Solution in Females With Primary Patellofemoral Osteoarthritis
In Brief
A clinical study evaluating nSTRIDE Autologous Protein Solution (APS) Kit for Patellofemoral Osteoarthritis. Completed, enrolled 52 participants across 1 site.
Detailed Summary
The purpose of this study is to evaluate clinical outcomes following a single injection of nSTRIDE Autologous Protein Solution in females with isolated patellofemoral osteoarthritis. A secondary objective of this study is to document the duration of treatment effect following nSTRIDE injection.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPatellofemoral Osteoarthritis
CountriesBelgium
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedNov 2015
Enrollment StartMar 2016
Primary CompletionJun 2018
TodayJul 2026
First PostedNov 20, 2015
Enrollment StartMar 1, 2016
Primary CompletionJun 1, 2018
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 10.6 years ago
Interventions
nSTRIDE Autologous Protein Solution (APS) Kitdevice
Intra-articular injection of APS