Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
402

Summary

Conditions
  • Avascular Necrosis
  • CDH
  • Osteoarthritis
  • Rheumatoid Arthritis
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Single Group AssignmentMasking: Single (Participant)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 80 years
Gender
Both males and females

Description

The clinical research results for the Trinity™ BIOLOX delta™ Ceramic-on-Ceramic Total Hip System will be compared to the control device Clinical success is based upon Harris Hip Scores to evaluate functional status, adverse events, radiological assessments and no device failure (defined as removal, ...

The clinical research results for the Trinity™ BIOLOX delta™ Ceramic-on-Ceramic Total Hip System will be compared to the control device Clinical success is based upon Harris Hip Scores to evaluate functional status, adverse events, radiological assessments and no device failure (defined as removal, replacement, or modification of any device component).

Tracking Information

NCT #
NCT01921309
Collaborators
Not Provided
Investigators
Study Director: Kathy Trier, Ph.D. Corin