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iAssist vs. Conventional Instrumentation in Total Knee Arthroplasty

NCT03111407 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 72

Last updated 2021-04-13

Study results available
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Summary

The purpose of this prospective study is to evaluate Zimmer® iASSIST™ with respect to radiographic, clinical and economic outcomes and compared to conventional instrumentation in primary total knee arthroplasty (NexGen or Persona knee implants).

Conditions

Interventions

PROCEDURE

total knee arthroplasty

surgical procedure in which damaged parts of the knee joint are replaced with an implant.

Sponsors & Collaborators

  • Zimmer, GmbH

    lead INDUSTRY

Principal Investigators

  • Paola Vivoda, Ass.Direct · Zimmer Biomet

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-04-30
Primary Completion
2018-12-31
Completion
2018-12-31

Countries

  • Spain
  • Switzerland

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03111407 on ClinicalTrials.gov