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Clinical Trial

14022 ATTUNE Cementless RP Clinical Performance Evaluation

NCT: NCT02839850 · ACTIVE_NOT_RECRUITING

NCT IDNCT02839850
StatusACTIVE_NOT_RECRUITING
Start Date2016-09-01
Completion2027-09-01
SponsorDePuy Orthopaedics (INDUSTRY)
First posted
Last updated

Brief Summary

The primary objective of this study is to examine the change from pre-operative baseline to two year postoperative functional performance improvement for the ATTUNE primary, cementless TKA RP system as measured with the KOOS questionnaire (KOOS-ADL sub-score). This will be carried out for two configurations: cruciate retaining rotating platform (ATTUNE Cementless CR RP) and posterior stabilized rotating platform (ATTUNE Cementless PS RP).

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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