- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01831401
A Study Investigating the Effect of Patient Pelvic Positioning and Method of Acetabular Component Insertion on Acetabular Component Inclination During Total Hip Arthroplasty (THA)
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
Status
Conditions
Intervention / Treatment
- Procedure: Operating table position 0° head down (Horizontal)
- Device: Standard straight acetabular component introducer without alignment guide.
- Device: Modified 35° acetabular component introducer.
- Device: Inclinometer-assisted acetabular component introducer.
- Procedure: Operating table position 7° head down.
- Procedure: Operating table position Y° head down
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
County Antrim
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Belfast, County Antrim, United Kingdom, BT9 7JB
- Musgrave Park Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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:
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Radiological acetabular component inclination will be measured on the routine post-operative pelvic x-ray, usually within 48 hrs from time of surgery.
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|
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:
|
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
Sponsor
Collaborators
Investigators
- Principal Investigator: David E Beverland, MD FRCS(Orth), Musgrave Park Hospital / Belfast Health & Social Care Trust
Publications and helpful links
General Publications
- Hill JC, Gibson DP, Pagoti R, Beverland DE. Photographic measurement of the inclination of the acetabular component in total hip replacement using the posterior approach. J Bone Joint Surg Br. 2010 Sep;92(9):1209-14. doi: 10.1302/0301-620X.92B9.24476.
- O'Neill CKJ, Magill P, Hill JC, Patterson CC, Molloy DO, Gill HS, Beverland DE. Correction of pelvic adduction during total hip arthroplasty reduces variability in radiographic inclination: findings of a randomised controlled trial. Hip Int. 2018 May;28(3):240-245. doi: 10.1177/1120700018777480.
- O'Neill CKJ, Hill JC, Patterson CC, Molloy DO, Gill HS, Beverland DE. Reducing variability in apparent operative inclination during total hip arthroplasty: findings of a randomised controlled trial. Hip Int. 2018 May;28(3):234-239. doi: 10.1177/1120700018777485.
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
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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