Patient Outcomes Using HIP7 Software as Compared to Conventional THA

Status Withdrawn

Clinical Trial Summary

The study is designed to demonstrate how Hip7 software can lead to improved patient outcomes compared to conventional procedures with standard instrumentation for total hip arthroplasties (THA) surgery.

Clinical Trial Description

This study is a prospective, multi-center, randomized, controlled clinical study in total hip arthroplasties (THA) surgery. The subjects meeting the inclusion/exclusion criteria specified in the protocol will receive THA using either Hip7 software or conventional instrumentation. The clinical follow-up evaluation will be performed preoperatively (Baseline), operatively, 6 weeks, 6 and 12 months after surgery using patient reported outcome measures regarding their general health, hip and physical abilities, quality of life and pain level. ;

Study Design

Related Conditions & MeSH terms

Hip Replacement

Clinical Trial Details

NCT number	NCT04989998
Study type	Interventional
Source	Smith & Nephew, Inc.
Contact
Status	Withdrawn
Phase	N/A
Start date	September 30, 2021
Completion date	October 31, 2024

View Details

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