Skip to content

Ceramic-on-Ceramic Total Hip Arthroplasty and Squeaking: Influence of Component Design

Ceramic-on-Ceramic Total Hip Arthroplasty and Squeaking: A Prospective, Blinded, Randomized Clinical Trial of Influence of Component Design

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01420900
Enrollment
204
Registered
2011-08-22
Start date
2011-09-30
Completion date
2017-11-03
Last updated
2017-11-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hip Arthrosis

Brief summary

The investigators want to examine if specific acetabular liner designs can be a contributing factor to audible squeaking associated with CoC bearings. The aim of the present study is to compare two different designed and well documented acetabular component systems with reference to squeaking and other noises from the hip.

Interventions

DEVICETHA with ABG II / Trident

Surgery with total hip arthroplasty in the form of ABG II / Trident

DEVICETHA with CLS / Trilogy

Surgery with total hip arthroplasty in the form of CLS / Trilogy

Sponsors

Vejle Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* All patients scheduled for uncemented THA under the age of 65 years.

Exclusion criteria

* Patients with the following diagnoses of the hip: Recent femoral fracture, sequelae from older femoral fracture, acetabular fracture, and traumatic dislocation of the hip. * Patients without ability to give informed consent and/or willingness to participate in the follow-up protocol. * Severely impaired level of function due to other physical deficiencies than the hip. * Mental disability that could impair a patient's decision-making capability of giving informed consent and not enabling valid data collection. * Earlier primary THA or revision THA in the contralateral hip. * Pathology requiring another prosthesis concept than the below mentioned. * Body mass index greater than 35.

Design outcomes

Primary

MeasureTime frame
All noises from THAOne year

Secondary

MeasureTime frame
Life qualityOne year

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026