- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03850665
Comparison of Functional Outcome in Patients After Hip Arthroplasty Depending on Surgical Approach
Comparison of Early Objective and Subjective Outcome in Patients After Hip Arthroplasty, Operated From Direct Anterior, Posterolateraland Anterolateral Approach: Prospective Randomized Clinical Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Patients with primary hip osteoarthritis will be included in a randomized controlled trial and assigned to total hip arthroplasty using one the of hip approaches: anterior or anterolateral. Subjects will be assessed preoperative and 3 and 12 moths postoperative.
Biomechanical gait parameters will be collected using tree-dimensional motion analysis system "BTS SMART".
Evaluation of the function of the middle gluteal muscle with superficial EMG (sEMG) percutaneous surface electromyography. Fatigue assessment (mean frequency and amplitude) of the gluteus medius muscle during isometric muscle contraction.
Balance and coordination as well as fall risk will be assessed with use of dynamometric Biodex Balance platform. The study will determine the values of individual indicators: general stability index (OWS), anterior-posterior stability index (APW), the median lateral stability index (MLW) and the fall risk index (RU).
Subjective assessment will be conducted with use of Visual Analogue Scale, WOMAC Index, Oxford Hip Score, The Short Form-36 (SF-36) and Harris Hip Score
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Warsaw, Poland
- Orthopaedics and Rehabilitation Department, Medical University of Warsaw
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Mazowieckie
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Warsaw, Mazowieckie, Poland
- Department of Orthopedics and Rehabilitation, Medical University of Warsaw
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- patient's consent for anticipation in the study
- BMI less than 35
- ability to walk the distance of 10m and stand up from the chair
- arthroplasty in one hip
Exclusion Criteria:
- patient's lack of consent for anticipation in the study
- neurological diseases
- balance disorders
- reoperations in the area of endoprosthesis
- muscles diseases
- rheumatic diseases (rheumatoid arthritis, ankylosing spondylitis)
- dizziness, vasovagal syncope
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Direct Anterior Approach (DAA)
Direct Anterior Approach surgery to replace the hip.
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Direct Anterior Approach surgery to replace the hip.
Anterolateral approach surgery to replace the hip.
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Active Comparator: Anterolateral approach
Anterolateral Approach surgery to replace the hip.
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Direct Anterior Approach surgery to replace the hip.
Anterolateral approach surgery to replace the hip.
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Active Comparator: Posterolateral approach
Posterolateral Approach surgery to replace the hip.
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Direct Anterior Approach surgery to replace the hip.
Anterolateral approach surgery to replace the hip.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in biomechanical gait parameters
Time Frame: from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
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Done by a biomechanics lab for patients to test their hip movements
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from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
|
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Gluteus medius muscle fatigue
Time Frame: from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
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Surface Electromyographic analysis performed for testing gluteus medius activity
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from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
|
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Change from baseline in Hip disability and Osteoarthritis Outcome Score (HOOS) activities of daily living (ADL)
Time Frame: from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
|
This asks the patient how their hip functions during their daily life. It has 5 subscales measuring Pain, Symptoms, ADL, Sports/Recreation and Quality of Life (which is calculated using all the subscores). Each subscale is calculated using the mean score, with each score range being from 0 to 4. The subscore is normalized such that the lower the number the more extreme the problem is. To calculate Quality of Life, the mean of the other 4 subscores are taken to calculate the score. This asks the patient how their hip functions during their daily life. It has 5 subscales measuring Pain, Symptoms, ADL, Sports/Recreation and Quality of Life (which is calculated using all the subscores). Each subscale is calculated using the mean score, with each score range being from 0 to 4. The subscore is normalized such that the lower the number the more extreme the problem is. To calculate Quality of Life, the mean of the other 4 subscores are taken to calculate the score. |
from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
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Change in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)
Time Frame: from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
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This measures health status as it relates to the hip.
There are 3 subscales, pain which score ranges from 0-20, stiffness range from 0-8, physical function ranging from 0-68.
The total score is just added up from the subscales.
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from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
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Change in Oxford scale
Time Frame: from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
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The Oxford scale is a physiotherapist objective-rated scale to asses muscle strength against the resistance.
It is graded from 0 (flicker of movement) to 5 (Through full range actively against strong resistance)
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from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
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Change in SF-36 scale
Time Frame: from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
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The SF-36 is a participant self-rated questionnaire that is a general measure of perceived health status comprising 36 questions, which yields an 8-scale health profile.
The vitality sub-score assesses energy and fatigue, and ranges from 0 (worst) - 100 (best).
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from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
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Change in Visual Analog Scale (VAS) scale
Time Frame: from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
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To measure pain.
This is a line with left most end representing no pain with the rightmost representing extreme pain.
The participant puts a line where they feel that day and it is measured with a ruler to determine score out of 100.
The line is 100mm long.
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from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
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Change in biomechanical gait balance
Time Frame: from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
|
Done by a biomechanics lab for patients to test their gait balance
|
from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
|
|
Change in biomechanical coordination
Time Frame: from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
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Done by a biomechanics lab for patients to test their hip movements coordination
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from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Radiological analysis of implants positioning
Time Frame: from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
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To measure angles associated with proper implants positioning
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from baseline (can be measured anytime to a maximum of one month before surgery) to 3 and 12 months post-operatively
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Artur Stolarczyk, Ph. D, Orthopaedics and Rehabilitation Department, Medical University of Warsaw
- Principal Investigator: Bartosz Maciąg, Orthopaedics and Rehabilitation Department, Medical University of Warsaw
Publications and helpful links
General Publications
- McConnell S, Kolopack P, Davis AM. The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC): a review of its utility and measurement properties. Arthritis Rheum. 2001 Oct;45(5):453-61. doi: 10.1002/1529-0131(200110)45:53.0.co;2-w. No abstract available.
- Mariconda M, Galasso O, Costa GG, Recano P, Cerbasi S. Quality of life and functionality after total hip arthroplasty: a long-term follow-up study. BMC Musculoskelet Disord. 2011 Oct 6;12:222. doi: 10.1186/1471-2474-12-222.
- Sinha A, Twycross-Lewis R, Small C, Morrissey D, Maffulli N. Motion analysis as an outcome measure for hip arthroplasty. Surgeon. 2011 Oct;9(5):284-91. doi: 10.1016/j.surge.2011.02.002. Epub 2011 Mar 13.
- Demos HA, Rorabeck CH, Bourne RB, MacDonald SJ, McCalden RW. Instability in primary total hip arthroplasty with the direct lateral approach. Clin Orthop Relat Res. 2001 Dec;(393):168-80. doi: 10.1097/00003086-200112000-00020.
- Wylde V, Blom AW, Bolink S, Brunton L, Dieppe P, Gooberman-Hill R, Grimm B, Mann C, Lenguerrand E. Assessing function in patients undergoing joint replacement: a study protocol for a cohort study. BMC Musculoskelet Disord. 2012 Nov 13;13:220. doi: 10.1186/1471-2474-13-220.
- Cheng TE, Wallis JA, Taylor NF, Holden CT, Marks P, Smith CL, Armstrong MS, Singh PJ. A Prospective Randomized Clinical Trial in Total Hip Arthroplasty-Comparing Early Results Between the Direct Anterior Approach and the Posterior Approach. J Arthroplasty. 2017 Mar;32(3):883-890. doi: 10.1016/j.arth.2016.08.027. Epub 2016 Aug 31.
- Queen RM, Schaeffer JF, Butler RJ, Berasi CC, Kelley SS, Attarian DE, Bolognesi MP. Does surgical approach during total hip arthroplasty alter gait recovery during the first year following surgery? J Arthroplasty. 2013 Oct;28(9):1639-43. doi: 10.1016/j.arth.2013.02.008. Epub 2013 Mar 19.
- Wesseling M, Meyer C, Corten K, Simon JP, Desloovere K, Jonkers I. Does surgical approach or prosthesis type affect hip joint loading one year after surgery? Gait Posture. 2016 Feb;44:74-82. doi: 10.1016/j.gaitpost.2015.11.009. Epub 2015 Nov 23.
- Foucher KC, Wimmer MA, Moisio KC, Hildebrand M, Berli MC, Walker MR, Berger RA, Galante JO. Time course and extent of functional recovery during the first postoperative year after minimally invasive total hip arthroplasty with two different surgical approaches--a randomized controlled trial. J Biomech. 2011 Feb 3;44(3):372-8. doi: 10.1016/j.jbiomech.2010.10.026. Epub 2010 Nov 13.
- Rosenlund S, Broeng L, Overgaard S, Jensen C, Holsgaard-Larsen A. The efficacy of modified direct lateral versus posterior approach on gait function and hip muscle strength after primary total hip arthroplasty at 12months follow-up. An explorative randomised controlled trial. Clin Biomech (Bristol, Avon). 2016 Nov;39:91-99. doi: 10.1016/j.clinbiomech.2016.09.011. Epub 2016 Sep 30.
- Yue C, Kang P, Pei F. Comparison of Direct Anterior and Lateral Approaches in Total Hip Arthroplasty: A Systematic Review and Meta-Analysis (PRISMA). Medicine (Baltimore). 2015 Dec;94(50):e2126. doi: 10.1097/MD.0000000000002126.
- Beaulieu ML, Lamontagne M, Beaule PE. Lower limb biomechanics during gait do not return to normal following total hip arthroplasty. Gait Posture. 2010 Jun;32(2):269-73. doi: 10.1016/j.gaitpost.2010.05.007. Epub 2010 Jun 11.
- Bennett D, Humphreys L, O'Brien S, Kelly C, Orr JF, Beverland DE. Gait kinematics of age-stratified hip replacement patients--a large scale, long-term follow-up study. Gait Posture. 2008 Aug;28(2):194-200. doi: 10.1016/j.gaitpost.2007.11.010. Epub 2008 Feb 19.
- Calo L, Rabini A, Picciotti PM, Laurino S, Passali GC, Ferrara PE, Maggi L, Piazzini DB, Specchia A, Frasca G, Ronconi G, Bertolini C, Scarano E. Postural control in patients with total hip replacement. Eur J Phys Rehabil Med. 2009 Sep;45(3):327-34. Epub 2009 Feb 11.
- Soderman P, Malchau H, Herberts P. Outcome of total hip replacement: a comparison of different measurement methods. Clin Orthop Relat Res. 2001 Sep;(390):163-72. doi: 10.1097/00003086-200109000-00019.
- Kalairajah Y, Azurza K, Hulme C, Molloy S, Drabu KJ. Health outcome measures in the evaluation of total hip arthroplasties--a comparison between the Harris hip score and the Oxford hip score. J Arthroplasty. 2005 Dec;20(8):1037-41. doi: 10.1016/j.arth.2005.04.017.
- Wylde V, Learmonth ID, Cavendish VJ. The Oxford hip score: the patient's perspective. Health Qual Life Outcomes. 2005 Oct 31;3:66. doi: 10.1186/1477-7525-3-66.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- THA/ Warsaw MU
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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