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Direct Anterior Approach Versus Direct Lateral Approach in Total Hip Arthroplasty

Not Applicable
Completed
Conditions
Coxarthrosis
Interventions
Procedure: direct anterior approach
Procedure: direct lateral approach
Registration Number
NCT02719236
Lead Sponsor
Iuliu Hatieganu University of Medicine and Pharmacy
Brief Summary

The purpose of this study is to compare the direct anterior approach and the direct lateral approach in primary total hip arthroplasty, regarding the postoperative function and pain, complications, radiological finds (X-ray), postoperative hemorrhage, markers for muscle damage (i.e creatine kinase (CK), lactate dehydrogenase(LDH/LD) , aspartate aminotransferase(AST), C-reactive protein (CRP),Troponin and Myoglobin) or other clinical outcomes.

Detailed Description

This is a prospective randomised controlled clinical trial and follow-up study comparing primary total hip arthroplasty performed either through a direct anterior approach or a lateral approach. At our hospital(i.e. Emergency County Hospital Cluj-Napoca), the lateral transgluteal approach was standard for more than 40 years. Starting 2008,the minimally invasive anterior approach was gradually implemented with the aim to facilitate early rehabilitation and improve functional results. Reduced blood loss, earlier functional recovery, low dislocation rates and shorter stays in hospital have been attributed to the muscle-sparing properties of the anterior approach.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
112
Inclusion Criteria
  • Clinical and radiological diagnosis of coxarthrosis
  • Those deemed capable of giving informed consent, understanding the aims of the study and expressing willingness to comply with the post-operative review programme.
Exclusion Criteria
  • Previous surgery on affected hip
  • The patient has inflammatory arthritis.
  • The patient has any type of infection.
  • The subject has a known metal allergy.
  • Patients with co-existent ipsilateral knee disease or back problems
  • Those with a known co-existent medical condition where death is anticipated within five years due to the pre-existing medical condition.
  • Patients requiring bilateral hip replacement.
  • Patient with active major psychiatric illness
  • Patients whose body mass index (BMI; kg/m2) >35.
  • Patients with active or suspected infection or sepsis.
  • Patients with renal failure and/or renal insufficiency.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Direct anterior approachdirect anterior approachPrimary total hip arthroplasty using a direct anterior approach
Direct lateral approachdirect lateral approachPrimary total hip arthroplasty using a direct lateral approach
Primary Outcome Measures
NameTimeMethod
Muscle damage assay using Myoglobin biomarkerDay of surgery

Before surgery, Myoglobin(ng/mL) baseline value is acquired in the morning, prior to any physical activity. Myoglobin value postoperatively is acquired at the 6 hour mark, when it reaches peak level. The change from baseline of the biomarker is calculated considering patient haemodilution.

Muscle damage assay using Troponin T biomarkerDay of surgery

Before surgery, Troponin T(pg/mL) baseline value is acquired in the morning ,prior to any physical activity.Troponin T(TnT) value postoperatively is acquired at the 6 hour mark, when it reaches peak level. The change from baseline of the biomarker is calculated considering patient haemodilution.

Secondary Outcome Measures
NameTimeMethod
Post Operative Pain Medication Usagefirst 7 postoperative days - on a daily basis and then weekly for a 3 months period

Postoperative, the amount of analgetics used by each patient is quantified (converted to opioid equivalent doses)

Functional outcome using the 36-Item Short Form Health Survey (SF-36)preoperative,and at follow-up visits at 6 weeks, 3 months, 6 months, 12 months and 24 months

The SF-36 Survey consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability.The eight sections are: vitality,physical, functioning,bodily pain,general health perceptions,physical role functioning,emotional role functioning, social role functioning and mental health.The objective is to assess the dynamics of patient clinical recovery comparing the SF-36 survey at predetermined follow-up visits and pre-op.

Muscle damage assay using Aspartate aminotransferase (AST)Day of operation and next 7 consecutive days

Aspartate aminotransferase (AST) is found in the liver, heart, skeletal muscle, kidneys, brain, and red blood cells. Serum AST level can be measured clinically as biomarker for muscle health. Baseline value is acquired before surgery. AST is measured daily, the first post-op week,in the morning, to avoid physiological circadian variations.

radiological assessment of cup and stem osteointegration in the replaced hip12 months postoperative

The outcome measured is correct component osteointegration of the acetabular component and femoral stem using standard X-ray of the replaced hip.

radiological assessment of stem positioning in the replaced hipfirst day postoperative

Using standard X-ray of the hip , placement of the stem is assessed on a Anterior-Posterior view (AP) and a Rolled Lateral view. The outcome measured is correct component placement, within the accepted range.

Functional outcome using Harris Hip Scorepreoperative,and at follow-up visits at 6 weeks, 3 months, 6 months, 12 months and 24 months

The postoperative rate of improvement in functional outcome, measured by the Harris Hip Score (HHS). The HHS was developed to assess the results of hip surgery and is intended to evaluate pain, function, range of motion and absence of deformity, with a range of possible outcomes from 0 to 100(\<70 Poor ;70 - 79 Fair; 80-89 Good; 90 -100 Excellent). The objective is to assess the dynamics of patient clinical recovery comparing functional outcome using HHS at predetermined follow-up visits and pre-op.

Muscle damage - Creatine kinase (CK)Day of operation and next 7 consecutive days

Creatine kinase (CK) - also known as creatine phosphokinase (CPK) or phospho-creatine kinase - is an enzyme expressed by various damaged tissues. Baseline value is acquired before surgery.CK-total is measured daily, the first post-op week,in the morning, to avoid physiological circadian variations.

Functional outcome using the 20-meters-timed-walk(66 feet) testat follow-up visits at 6 weeks, 3 months, 6 months, 12 months and 24 months

Performance-based measures such as the 20 meters timed walk (20MTW) Test quantify performance with tasks mimicking activities of daily living, as opposed to relying on individuals perception of performance.Hence, they may provide a more objective measure of functional capacity. The test consists in timing the patient while walking a distance of 20 meters(66feet).

Pain assessment using the Visual Numeric Scalefirst 7 postoperative days - on a daily basis and then weekly for a 3 months period

The pain felt by the patient is measured using the Visual Numeric Scale(VNS) consisting of a scale from 0-10 (0 = no pain; 10 = worst imaginable pain).

Functional outcome using the Oxford Hip Score Surveypreoperative,and at follow-up visits at 6 weeks, 3 months, 6 months, 12 months and 24 months

The Oxford hip score (OHS) is a joint specific outcome measure tool designed to assess disability in patients undergoing total hip replacement (THR).The OHS is a patient-centred questionnaire that is designed to assess functional ability, and pain from the patient's perspective. It is a short, twelve-item questionnaire. Each item has five response categories, given a score of between 1-5 (low disability to high disability). Scoring involves summating the total for each item to produce a final score between 12-60, with a higher score indicating greater disability The objective is to assess the dynamics of patient clinical recovery comparing the OHS at predetermined follow-up visits and pre-op.

Functional outcome using the Stair Climbing Test (SCT)at follow-up visits at 6 weeks, 3 months, 6 months, 12 months and 24 months

Performance-based measures such as the Stair Climbing Test (SCT) quantify performance with tasks mimicking activities of daily living, as opposed to relying on individuals perception of performance.Hence, they may provide a more objective measure of functional capacity. The test consists in timing the patient while climbing 10 steps.

radiological assessment of cup positioning in the replaced hipfirst day postoperative

Using standard X-ray of the hip - Placement of the acetabular component (inclination and version) is assessed on a Anterior-Posterior view (AP) and a Rolled Lateral view. The outcome measured is correct component placement, within the accepted range.

Muscle damage - Lactate dehydrogenase (LDH or LD)Day of operation and next 7 consecutive days

Lactate dehydrogenase (LDH or LD) is an enzyme found in nearly all living cells.LDH is expressed extensively in body tissues, such as blood cells and heart muscle. Because it is released during tissue damage, it is a marker of common injuries and disease such as surgical muscle damage. Baseline value is acquired before surgery. LDH is measured daily, the first post-op week,in the morning, to avoid physiological circadian variations.

Length of Hospital Stay10 days postoperative

The length of stay will be determined for each patient,to evaluate and compare the percentage of patients who are able to be discharged in less than 5 days after undergoing total hip arthroplasty through either a direct anterior or lateral approach, utilizing the identical post operative protocol for physical recovery.

Trial Locations

Locations (1)

Emergency County Hospital Cluj-Napoca, Orthopedics and Trauma Clinic

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Cluj-Napoca, Cluj, Romania

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