Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03900039
Other study ID # #04-025
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 26, 2005
Est. completion date March 26, 2019

Study information

Verified date April 2019
Source St. Michael's Hospital, Toronto
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to assess the ideal bearing surfaces in hip replacement by comparing 4 different combinations. In a hip replacement this means what the head and the socket liner are made of.


Description:

In hip replacements, arguably the most important thing for survivorship is what rubs against what.

Traditionally surgeons used metal (Cobalt-Chrome) against a conventional polyethylene (plastic). More recently (around 15 years ago) a newer more dense type of polyethylene (called XLPE) had been developed and a new type of head called Oxidized Zirconium was also developed.

In this trial, adults who were undergoing hip replacements were randomized assigned into one of the four groups:

Group 1: old plastic vs metal head Group 2: Old plastic against Oxidized Zirconium Group 3: New plastic versus metal head Group 4 New plastic vs Oxidized Zirconium

All patients were followed up for a minimum of 10 years to assess which group wore the most amount of polyethylene and which group had the best survival rate.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date March 26, 2019
Est. primary completion date July 26, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- All adults with no history of cancer, infection of the hip and with the capacity to make informed consent for the trial

Exclusion Criteria:

- those under the age of 18 and over 65. Those with a history of cancer and infection. Those without the capacity to make an informed consent.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Highly Cross Linked Polyethylene and oxidized zirconium femoral head
Differing bearing surfaces: Conventional polyethylene versus cobalt Chrome heads Conventional polyethylene versus Oxidized Zirconium heads Highly Cross-linked polyethylene versus Cobalt Chrome heads Highly Cross-linked polyethylene versus Oxidized Zirconium heads

Locations

Country Name City State
Canada St. Michael's Hospital Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
St. Michael's Hospital, Toronto

Country where clinical trial is conducted

Canada, 

References & Publications (2)

Atrey A, Ward SE, Khoshbin A, Hussain N, Bogoch E, Schemitsch EH, Waddell JP. Ten-year follow-up study of three alternative bearing surfaces used in total hip arthroplasty in young patients: a prospective randomised controlled trial. Bone Joint J. 2017 Dec;99-B(12):1590-1595. doi: 10.1302/0301-620X.99B12.BJJ-2017-0353.R1. — View Citation

Rames RD, Stambough JB, Pashos GE, Maloney WJ, Martell JM, Clohisy JC. Fifteen-Year Results of Total Hip Arthroplasty With Cobalt-Chromium Femoral Heads on Highly Cross-Linked Polyethylene in Patients 50 Years and Less. J Arthroplasty. 2019 Feb 5. pii: S0 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Wear rates of polyethylene over 10 years Linear and volumetric wear were measured in the most recent radiographs using a computer software package (Polyware Rev. 5; Draftware). Over 10 years of wear rates
Secondary Survivorship of implant combinations Assess linear and volumetric wear to assess if those bearing surfaces require to be revised (exchanged) during the experimental period in one group more than the others over 10 years
See also
  Status Clinical Trial Phase
Active, not recruiting NCT05181566 - Metal Ion Levels in Total Hip Arthroplasty (THA) With Modular Dual Mobility Cup Compared to Conventional THA N/A
Completed NCT04490304 - The Analysis of Posterior Soft Tissue Repair Durability N/A
Completed NCT05974501 - Pre vs Post Block in Total Knee Arthroplasty (TKA) Phase 4
Completed NCT04565093 - Efficacy of iPACK After Unilateral TKA N/A
Recruiting NCT05845021 - Surgeon-Initiated Bone Health Referral Pathway in Patients Undergoing Lower Extremity Arthroplasty N/A
Recruiting NCT03306810 - Recognition and Treatment of Dysglycemia. AGS - Acute Glucose Service N/A
Completed NCT04289025 - Modelling and AI Using Sensor Data to Personalise REHABilitation Following Joint Replacement N/A
Not yet recruiting NCT06469177 - Patient Centered Post-Op Pain Management Software Tool Interventional Study Verses Standard of Care N/A
Not yet recruiting NCT05014932 - Evaluation of Noise Induced by Ceramic-ceramic Friction Torques of Total Hip Prostheses With Customized Femoral Stem
Active, not recruiting NCT04437888 - Intraoperative Ketamine for Patients Undergoing Total Joint Arthroplasty Early Phase 1
Completed NCT05420194 - Assessment of Postural Stability in Patients With Total Knee Arthroplasty
Completed NCT03269760 - Multimodal Sleep Pathway for Shoulder Arthroplasty Phase 1
Completed NCT03289247 - Tissue Adhaesive in Wound Closure Following Primary Total Knee Arthroplasty N/A
Completed NCT04433962 - Investigation of the Effects of Balance Training on Balance and Functional Status Patients With Total Hip Arthroplasty N/A
Recruiting NCT06025448 - Is MIO-RSA Noninferior to BIO-RSA When it Comes to Mechanical Implant Stability? N/A
Recruiting NCT05459259 - Physiotherapy for Arthrofibrosis Following Knee Replacement.
Not yet recruiting NCT05736666 - Treadmill Perturbation Training for Fall Prevention After Total Knee Replacement N/A
Active, not recruiting NCT03692364 - Evaluation of Metal-on-conventional-polyethylene vs Ceramic-on-ceramic Articulating Surfaces in Total Hip Arthroplasty N/A
Completed NCT05013879 - Kinesiotape for Edema After Bilateral Total Knee Arthroplasty N/A
Completed NCT04120324 - Incidence of 30 Day Return to Hospital Following Same Day Discharge Total Hip Arthroplasty