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Clinical Trial Summary

The purpose of this study is to compare reduction positon maintenance rate at 3 weeks post-operatively between patients operated with Anterior Support Screw (AS2) and without AS2 technique in RCT setting. Total 240 cases(each arm 120 cases) will be enrolled at maximum 15sites, total study duration is 22months.


Clinical Trial Description

Objective: To compare fracture reduction maintenance rate at 2-3weeks post-operatively between patients operated with AS2 (investigational group) and patients operated without AS2 (Control group) using same implant system (ZNN CM Asia, Zimmer Biomet).

Endpoint: Primary: The rate of reduction position maintenance at 2-3 weeks post-operatively. Secondary: Surgery time / fracture type / postoperative reduction position / CT assessment / Safety information ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03196193
Study type Interventional
Source Zimmer Biomet
Contact
Status Completed
Phase N/A
Start date March 21, 2017
Completion date April 9, 2020

See also
  Status Clinical Trial Phase
Active, not recruiting NCT04498715 - Trochanteric Femur Fracture Operated With Dynamic Hip Screw System (DHS) Augmented With a Biphasic Apatite Sulphate Combined With Systemic or Local Bisphosphonate N/A
Recruiting NCT06135298 - FARE Augmentation of Proximal Femoral Fractures With CaS/HA and Systemic ZA Phase 4