RECRUITING

Dual Mobility Acetabular Cups in Revision TJA

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The aim of this study is to the compare clinical outcomes of patients undergoing a revision total hip arthroplasty (THA) with the use of a dual mobility bearing versus a single bearing design with the use of a large femoral head (36mm or 40mm). We hypothesize the use of dual-mobility components in revision THA will be associated with a lower dislocation rate in the first year following surgery.

Official Title

Dual Mobility Acetabular Cups in Revision TJA

Quick Facts

Study Start:2017-09-01
Study Completion:2035-03-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04090359

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Any patient older than 18 years of age scheduled for a revision THA, including revision of both components, conversion of a hip resurfacing to THA, conversion of a hemiarthroplasty to THA, and revision of single components which allow implantation of dual-mobility bearings. In addition, patients undergoing reimplantation of a total hip arthroplasty following a two-stage revision for periprosthetic infection will also be included. Only patients with an acetabular shell diameter capable of accommodating at least a 36mm femoral head will be included.
  1. * Less than 18 years of age, primary THA,
  2. * conversion of non-arthroplasty femoral neck fracture fixation to THA,
  3. * patients unwilling to participate.
  4. * patients where the surgeon makes the intraoperative decision to use a constrained liner will be excluded.

Contacts and Locations

Study Contact

Craig Della Valle, MD
CONTACT
(312)432-2468
craig.dellavalle@rushortho.com
Anne DeBenedetti, BA
CONTACT
(312)432-2468
anne.debenedetti@rushortho.com

Study Locations (Sites)

New York University Medical Center
New York, New York, 10003
United States
Rothman Institute
Philadelphia, Pennsylvania, 19107
United States

Collaborators and Investigators

Sponsor: Rush University Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2017-09-01
Study Completion Date2035-03-01

Study Record Updates

Study Start Date2017-09-01
Study Completion Date2035-03-01

Terms related to this study

Additional Relevant MeSH Terms

  • Dislocation, Hip