A Study Investigating the Effect of Patient Pelvic Positioning and Method of Acetabular Component Insertion on Acetabular Component Inclination During Total Hip Arthroplasty (THA)

March 20, 2016 updated by: Professor David Beverland, Musgrave Park Hospital

A Randomised Controlled Study Investigating the Effect of Patient Pelvic Positioning and Method of Acetabular Component Insertion on Acetabular Component Inclination During Total Hip Arthroplasty (THA).

Total Hip Arthroplasty (THA) is one of the most commonly performed orthopaedic operations worldwide. The main aim is overall improvement in levels of patient pain and mobility. Such surgery involves implantation of both an acetabular and femoral component. With the patient in the lateral decubitus position, the Orthopaedic Surgeon assumes that the pelvis is in a neutral position with respect to all three body planes at the time of acetabular component implantation.

With regard to THA, the current orthopaedic literature demonstrates a clear relationship between acetabular component positioning, polyethylene wear and risk of dislocation. Problems with edge loading, stripe wear and squeaking are also associated with higher acetabular inclination angles, particularly in hard-on-hard bearing implants.

The important parameters of acetabular component positioning are depth, height, version and inclination.

Control of acetabular component inclination, particularly in the lateral decubitus position, is difficult and remains a challenge for the Orthopaedic Surgeon.

Accurate implantation of the acetabular component within the 'safe zone' of radiological inclination is dependent on:

  • Operative version
  • Operative inclination
  • Pelvic position (Primarily, but not exclusively, abduction / adduction.)

This study aims to investigate the effect of patient pelvic positioning and method of acetabular component insertion on acetabular component inclination during Total Hip Arthroplasty (THA).

Study Overview

Study Type

Interventional

Enrollment (Actual)

270

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • County Antrim
      • Belfast, County Antrim, United Kingdom, BT9 7JB
        • Musgrave Park Hospital

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.

Eligibility Criteria

Ages Eligible for Study

16 years to 100 years (ADULT, OLDER_ADULT, CHILD)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • All patients between the ages of 16 and 100 years awaiting primary Total Hip Arthroplasty the care of Professor D Beverland and Mr D Molloy in Musgrave Park Hospital will initially be invited to participate.

Exclusion Criteria:

  • Patients unable to provide fully informed consent.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Allocation: RANDOMIZED
  • Interventional Model: FACTORIAL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: 0° Head Down (horizontal) & Standard Introducer.
Operating table position 0° head down (horizontal) & standard straight acetabular component introducer without alignment guide.
EXPERIMENTAL: 0° Head Down (horizontal) & Modified 35° Introducer.
Operating table position 0°head down (horizontal) & modified 35° acetabular component introducer.
EXPERIMENTAL: 0°Head Down (horizontal) & Inclinometer-assisted Introducer.
Operating table position 0°head down (horizontal) & standard straight acetabular component introducer without alignment guide.
EXPERIMENTAL: 7° Head Down & Standard Introducer.
Operating table position 7° head down & standard straight acetabular component introducer without alignment guide.
EXPERIMENTAL: 7° Head Down & Modified 35° Introducer.
Operating table position 7° head down & modified 35° acetabular component introducer.
EXPERIMENTAL: 7° Head Down & Inclinometer-assisted Introducer.
Operating table position 7° head down & inclinometer-assisted acetabular component introducer.
EXPERIMENTAL: Y° Head Down & Standard Introducer.
Operating table position Y° head down (angle required to obtain vertical Transverse Pelvis Lines) & standard straight acetabular component introducer without alignment guide.
Operating table position Y° head down (angle required to obtain vertical Transverse Pelvis Lines).
EXPERIMENTAL: Y° Head Down & Modified 35° Introducer.
Operating table position Y° head down (angle required to obtain vertical Transverse Pelvis Lines) & modified 35°acetabular component introducer.
Operating table position Y° head down (angle required to obtain vertical Transverse Pelvis Lines).
EXPERIMENTAL: Y° Head Down & Inclinometer-assisted Introducer.
Operating table position Y° head down (angle required to obtain vertical Transverse Pelvis Lines) & inclinometer-assisted acetabular component introducer.
Operating table position Y° head down (angle required to obtain vertical Transverse Pelvis Lines).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Radiological acetabular component inclination.
Time Frame: Radiological acetabular component inclination will be measured on the routine post-operative pelvic x-ray, usually within 48 hrs from time of surgery.

The study has two primary aims, each with a different primary outcome.

The first primary aim is to investigate the effect of adjusting patient pelvic position in the transverse plane by using a head down position of the operating table.

This is to determine, when aiming for 35° of operative inclination, which operating table position most accurately achieves a target radiological inclination of 42° on the post-operative x-ray:

  1. 0° head down (Horizontal),
  2. 7° head down, or
  3. Y° head down (Angle required to obtain vertical Transverse Pelvic Lines).
Radiological acetabular component inclination will be measured on the routine post-operative pelvic x-ray, usually within 48 hrs from time of surgery.
Operative Acetabular Component Inclination.
Time Frame: Operative acetabular component inclination will be measured intra-operatively.

The study has two primary aims, each with a different primary outcome.

The second primary aim is to determine which of the three methods of acetabular component insertion most accurately allows the Orthopaedic Surgeon to obtain the desired operative inclination of 35° during THA when using a cementless cup:

  1. Standard straight introducer without any alignment guide,
  2. Modified 35° introducer with horizontal alignment guide, or
  3. Digital inclinometer assisted introducer.
Operative acetabular component inclination will be measured intra-operatively.

Secondary Outcome Measures

Outcome Measure
Time Frame
Proportion of cases in which the target radiological inclination of 42 +/- 5° is actually obtained.
Time Frame: Radiological acetabular component inclination will be measured on the routine post-operative pelvic x-ray, usually within 48 hrs from time of surgery.
Radiological acetabular component inclination will be measured on the routine post-operative pelvic x-ray, usually within 48 hrs from time of surgery.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: David E Beverland, MD FRCS(Orth), Musgrave Park Hospital / Belfast Health & Social Care Trust

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 Major Dates

Study Start

August 1, 2013

Primary Completion (ACTUAL)

April 1, 2014

Study Completion (ACTUAL)

April 1, 2014

Study Registration Dates

First Submitted

February 15, 2013

First Submitted That Met QC Criteria

April 10, 2013

First Posted (ESTIMATE)

April 15, 2013

Study Record Updates

Last Update Posted (ESTIMATE)

March 22, 2016

Last Update Submitted That Met QC Criteria

March 20, 2016

Last Verified

March 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • 12080DB-SW

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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