CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 95 enrolled
Drug / intervention
Sidus Stem-Free Total Shoulder Arthroplasty Systemdevice
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.

Search/NCT01878253
NCT01878253N/ACompleted

Multicenter Trial of the Sidus Stem-Free Shoulder Arthroplasty System

Zimmer Biomet·interventional·Posted Jun 14, 2013·Updated Jul 15, 2019

In Brief

A clinical study evaluating Sidus Stem-Free Total Shoulder Arthroplasty System for Osteoarthritis and 2 related conditions. Completed, enrolled 95 participants across 11 sites in 2 countries.

Detailed Summary

The purpose of this study is to determine if Sidus stem-free shoulder system is safe and effective when used in total shoulder replacement.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, United States
Collaborators--

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedJun 14, 2013
Enrollment StartJul 1, 2013
Primary CompletionMay 1, 2018
Study CompletionJan 1, 2019
TodayJul 2, 2026
Enrollment to primary: 4.8 yearsPosted 13.0 years ago

Interventions

Sidus Stem-Free Total Shoulder Arthroplasty Systemdevice