CClinicalTrials.gg
CompletedNCT02311166Updated Apr 8, 2021

Soft Tissue Pathology in Hip Dysplasia Before and After Periacetabular Osteotomy

An observational study in Hip Dysplasia, sponsored by University of Aarhus. Completed at 2 sites in Denmark. Per ClinicalTrials.gov, last updated 2021-04-08.

Sponsored by University of Aarhus · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Sex
All
01

Study summary

Introduction: The lack of congruence between the acetabulum and femoral head in hip dysplasia compromise the passive stability of the hip joint resulting in increased stress on the acetabular labrum, joint capsule and the muscles acting close to the hip joint. Soft tissue injury is present in hip dysplasia, and pathology of the iliopsoas muscle has been found in 18-50%. To our knowledge, no studies have systematically examined the prevalence of soft tissue pathology in hip dysplasia.

The overall aim of this research project is to examine soft tissue pathology in 100 patients with hip dysplasia prior to and one year after Periacetabular osteotomy (PAO).

Methods: Soft tissue pathology will be examined in a prospective cohort study on 100 patients with hip dysplasia prior to and one year after surgery. Pathology will be examined using ultrasonography and the Clinical Entities Approach that focus on pathology of the iliopsoas, adductors, rectus abdominis, gluteus medius and hamstrings. Furthermore, hip muscle strength is tested with a dynamometer, hip related health is measured with the Copenhagen Hip and Groin Outcome Score (HAGOS) and physical activity is measured with triaxial accelerometers during a period of 7 days.

Perspective: Is it possible to demonstrate pathology of the hip muscles and tendons applying clinical tests, muscle strength tests, and ultrasonography, as it has been found in sports-active people with groin pain, it will make sense to plan and test a specific training program focusing on the pathological soft tissue pathology.

Read the detailed description

Introduction

In hip dysplasia the acetabulum presents as shallow and oblique with insufficient coverage of the femoral head. Deformity of the femoral neck and head is common with bilateral affection in 54%. The lack of congruence between the acetabulum and femoral head compromise the passive stability of the hip joint resulting in increased increased stress on the acetabular labrum, joint capsule and the muscles acting close to the hip joint. The increased stress on soft tissue results in acetabular labrum injury in 49-94% of the patients with hip dysplasia scheduled for joint preserving surgery. Left untreated hip dysplasia may lead to development of early osteoarthritis; however, the osteoarthritic process can be prevented or delayed with the Periacetabular osteotomy (PAO).

Soft tissue injury is present in hip dysplasia, and pathology of the iliopsoas muscle has been found in 18-50%. The muscles acting close to the hip joint including the deep fibers of the iliopsoas and the iliocapsularis muscle are together with the acetabular labrum and joint capsule able to increase the dynamic stabilisation of the femoral head in the dysplastic and shallow acetabulum. The hip joint is beside the iliopsoas further stabilised by the adductors and the gluteus medius muscle. Sustained hip pain and immobilisation has a negative impact on the iliopsoas, psoas and the hip adductors in terms of atrophy and decreased hip muscle strength. In an experimental study design it was found that decreased force contribution from the gluteal muscles during hip extension and the iliopsoas muscle during hip flexion resulted in an increase in the anterior hip joint force. The increased anterior hip joint force may contribute to anterior hip pain, subtle hip instability and the development of anterior acetabular labral tears.

Patients with hip dysplasia are less physical active prior to PAO mainly due to groin pain. A decreased physical activity level is likely to have a negative impact on the muscles acting close to the hip joint with a possible increased risk of sustaining further acetabular labrum injury and/or overuse related to soft tissue pathology. After surgery, the risk of overuse related soft tissue pathology might be further increased due to surgery impact on muscles and tendons. If it is possible to demonstrate pathology of the hip muscles and tendons applying clinical tests, muscle strength tests, and ultrasonography, as it has been found in sports-active people with groin pain, it will make sense to plan and test a specific training program focusing on the pathological soft tissue pathology.

The overall aim of this research project is to examine soft tissue pathology in 100 patients with hip dysplasia prior to and one year after PAO.

Material and methods

Design Prospective cohort study on 100 patients with symptomatic and radiologically verified hip dysplasia with one year of follow-up.

Inclusion

  1. Diagnosis of hip dysplasia with a Wiberg´s Center-Edge (CE) angle \<25 degrees, and planned PAO surgery at Aarhus University Hospital

Exclusion

  1. Osteoarthritis grade ≥2 using Tönnis' classification
  2. Other hip conditions as Calvé Perthes and epiphysiolysis
  3. Surgery due to discus disease and spondylodesis and joint preserving and alloplastic surgery at the hip, knee or angle region
  4. Neurological and/or rheumatological conditions affecting the function of the hip joint
  5. Tenotomy of the iliopsoas tendon
  6. BMI > 40
  7. Cross-over sign (retroversion of the acetabulum)

Primary outcomes measures

  1. Soft tissue pathology of abnormal clinical entities of the iliopsoas, adductors, rectus abdominis, gluteus medius and hamstrings using a standardized and reliable examination protocol
  2. Soft tissue pathology of the iliopsoas, adductors, rectus abdominis, gluteus medius and hamstrings using a standardized ultrasonography protocol
  3. Hip related health measured with the reliable Copenhagen Hip and Groin Outcome Score (HAGOS) validated on patients with groin pain
  4. Physical activity measured with triaxial accelerometers during a period of 7 days on the following categories: rest, standing, walking, sit to stand (STS), cycling and running

Secondary outcome measures

  1. Isometric hip muscle strength of the hip flexors, hip abductors, hip adductors and hip extensors using a reliable standardized method
  2. Subjective visual analogue scale (VAS) at rest and during hip muscle strength tests
  3. Pain location registered on a pain-drawing
  4. Presence of internal snapping hip examined with a standardized examination test and ultrasonography
  5. Presence of intra-articular pathology examined with the Flexion/Abduction/External Rotation (FABER) and Flexion/Adduction/Internal Rotation (FADDIR) tests and ultrasonography of the hip joint
  6. Presence of lumbar and thoracic back pathology examined with the reliable Spine Springing Tests of the spinous process and processus transversi and of the sacrum
  7. Conjoint tendon pathology examined with palpation of the pubic tubercle and ultrasonography of the pubic tubercle

Procedure

Patients are included from the division of hip surgery at Aarhus University Hospital using the listed inclusion and exclusion criteria's. The patients complete the HAGOS questionnaire after informed written consent. Wiberg's center-edge (CE) angle, Tönnis' acetabular index (AI) angle, and osteoarthritis grade are measured on anteroposterior radiographs after inclusion and after surgery by the surgeon. Information from the hospital charts is used to record age, gender, unilateral or bilateral involvement and other pathologies. Baseline characteristics are registered using standardized questions including data on BMI, duration of pain and intake of analgesia. Pain is afterwards measured on 100 mm visual analogue scale (VAS) resting in sitting and lying, and furthermore registered on a pain drawing. Preferred physical activity and hours spend on primary and overall physical activity is registered using standardized questions.

Ultrasonography is carried out first with an ultrasound scanner (Noblus, Hitachi-Aloka Medical, Zug, Switzerland) using an 18 Megahertz (MHz) linear transducer.Then the standardized examination protocol of abnormal clinical entities is carried out. Examination of pain at the conjoint tendon, presence of lumbar and thoracic back pathology, examination of intra-articular pathology and evaluation of internal snapping hip follow this. The hip muscle strength is then carried out, and finally the physical activity sensor is attached, and the patients are informed on how to monitor duration of physical activity.

One year postoperative the following examination is carried out in the listed order: HAGOS, baseline characteristics, pain on a VAS scale, pain on a pain drawing, hours of physical activity, ultrasonography, abnormal clinical entities, pain at the conjoint tendon, presence of lumbar and thoracic back pathology, examination of intra-articular pathology, evaluation of internal snapping hip, hip muscle strength. Finally the physical activity sensor is attached and the patient informed.

Statistics

Stata 11 is used for statistic calculations, and results are presented as significant if p\<0.05.

Sample size

The present study is a descriptive study aiming to describe musculotendinous pathology in patients with hip dysplasia. This means that a power calculation is not feasible. On an annual basis approximately 140 periacetabular osteotomies is carried out on Aarhus University Hospital.

Allowing a lack of participation of 25 % it seems possible to include 100 patients during a period of one year. Based on this, a convenience sample of 100 patients is included to describe musculotendinous pathology in patients with hip dysplasia.

Ethics

The study was presented to the local research ethics the 14th of January 2014. The Committee waived the request of ethic approval, since the study according to Danish law does not require approval owing the observational design (Request 5/2014). All participants provided written consent prior to inclusion, and approval has been obtained from the Danish Data Protection Agency (Reference number: 1-16-02-47-14).

Economy and publicising

Financial support will be applied to internal and external funds. Both positive and negative results will be published in international journals and presented at conferences.

02

Conditions studied

  • Hip Dysplasia

Keywords

  • Hip dysplasia
  • Soft tissue
  • Hip
  • Self-report
  • Physical activity
03

In context

Hip Dislocation

141 studies on the registry are indexed under Hip Dislocation; 34 are open to participants now.

This study's enrollment of 100 is below the median of 150 across 45 observational studies indexed under Hip Dislocation.

Browse Hip Dislocation studies →

Lead sponsor

University of Aarhus is the lead sponsor of 1,274 studies on the registry; 183 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with a diagnosis of hip dysplasia receiving treatment at Aarhus University Hospital, Denmark.

Inclusion criteria

  1. Diagnosis of hip dysplasia with a Wiberg´s Center-Edge (CE) angle \<25 degrees, and planned PAO surgery at Aarhus University Hospital

Exclusion criteria

Exclusion Criteria:

  1. Osteoarthritis grade ≥2 using Tönnis' classification
  2. Other hip conditions as Calvé Perthes and epiphysiolysis
  3. Surgery due to discus disease and spondylodesis and joint preserving and alloplastic surgery at the hip, knee or angle region
  4. Neurological and/or rheumatological conditions affecting the function of the hip joint
  5. Tenotomy of the iliopsoas tendon
  6. BMI > 40
  7. Cross-over sign (retroversion of the acetabulum)
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Soft tissue pathology in the hip region (xamined with the Clinical Entities Approach)

    Soft tissue pathology will be examined with the Clinical Entities Approach examining pathology of the iliopsoas, adductors, rectus abdominis, gluteus medius and hamstrings using a standardized and reliable examination protocol

    Time frame: Prior to surgery and one year after surgery

  2. Soft tissue pathology of the hip region using a standardized ultrasonography protocol

    Soft tissue pathology of the iliopsoas, adductors, rectus abdominis, gluteus medius and hamstrings is examined using a standardized ultrasonography protocol.

    Time frame: Prior to surgery and one year after surgery

  3. Hip related self-reports of health (Copenhagen Hip and Groin Outcome Score (HAGOS)

    Hip related health measured with the reliable Copenhagen Hip and Groin Outcome Score (HAGOS) validated on patients with groin pain.

    Time frame: Prior to surgery and one year after surgery

  4. Physical activity during a period of 7 days (measured with triaxial accelerometers)

    Physical activity is measured with triaxial accelerometers during a period of 7 days on the following categories: rest, standing, walking, sit to stand (STS), cycling and running.

    Time frame: Prior to surgery and one year after surgery

Secondary outcomes

  1. Isometric hip muscle strength using a dynamometer

    Isometric hip muscle strength of the hip flexors, hip abductors, hip adductors and hip extensors using a dynamometer

    Time frame: Prior to surgery and one year after surgery

  2. Subjective visual analogue scale (VAS)

    Subjective visual analogue scale (VAS) at rest and during hip muscle strength tests.

    Time frame: Prior to surgery and one year after surgery

  3. Pain location registered on a pain-drawing

    In an anatomical picture of a human body the patients records pain areas on the drawing.

    Time frame: Prior to surgery and one year after surgery

  4. Presence of internal snapping hip (examined with a standardized examination test)

    Presence of internal snapping hip examined with a standardized examination test.

    Time frame: Prior to surgery and one year after surgery

  5. Presence of lumbar and thoracic back pathology

    Presence of lumbar and thoracic back pathology is examined with the reliable Spine Springing Tests of the spinous process and processus transversi and of the sacrum.

    Time frame: Prior to surgery and one year after surgery

  6. Conjoint tendon pathology

    Conjoint tendon pathology is examined with palpation of the pubic tubercle and ultrasonography of the pubic tubercle.

    Time frame: Prior to surgery and one year after surgery

Other outcomes

  1. Wiberg's center-edge (CE) angle

    CE angel is measured on anteroposterior radiographs

    Time frame: Prior to surgery and one year after surgery

  2. Tönnis' acetabular index (AI) angle

    Measured on anteroposterior radiographs

    Time frame: Prior to surgery and one year after surgery

  3. Osteoarthritis grade

    Measured on anteroposterior radiographs

    Time frame: Prior to surgery

  4. Duration of pain

    Time frame: Prior to surgery

  5. Intake of analgesia

    Time frame: Prior to surgery and one year after surgery

  6. Preferred physical activity and hours spend on this

    Time frame: Prior to surgery and one year after surgery

  7. Body Mass Index

    Time frame: Prior to surgery and one year after surgery

  8. Age

    Time frame: Prior to surgery

  9. Hours spend on general physical activity

    Time frame: Prior to surgery and one year after surgery

07

Study locations

2 sites
  • Department of Orthopaedics, Aarhus University Hospital
    Aarhus, 8000, Denmark
  • Department of Physiotherapy and Occupational Therapy, Aarhus University Hospital
    Aarhus, Dk-8000, Denmark
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 8, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02311166
Lead sponsor
University of Aarhus
Collaborators
University of Copenhagen
Responsible party
Sponsor
First posted
Dec 8, 2014
Start date
Apr 1, 2014
Primary completion
Sep 6, 2017
Completion
Sep 6, 2017
Last update
Apr 8, 2021

Study contacts

Kjeld Soballe, Prof. Dr.med
study chair · Department of Orthopaedic surgery, Aarhus University Hospital
Per Hölmich, Dr.med
study chair · Arthroscopic Center Amager, Amager University Hospital
Kristian Thorborg, MSc, PhD
study chair · Arthroscopic Center Amager, Amager University Hospital
Lars Bolvig, MD
study chair · Department of Orthopaedic surgery, Aarhus University Hospital
Stig S Jakobsen, MD
study chair · Department of Orthopaedic surgery, Aarhus University Hospital
Inger Mechlenburg, MSc, PhD
study director · Department of Orthopaedic surgery, Aarhus University Hospital

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2014. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion