Recruiting

Ethnic Norms of Knee Ligament Stiffness and Association with Osteoarthritis Before/After Treatment

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Study Aim

This study aims to observe and measure the stiffness of your knee ligaments using Shear Wave Elastography, and understand its association with osteoarthritis before and after treatment, focusing on different ethnic groups.

What is being collected

Procedure Data

+ procedure Data

+ procedure Data

Collected from today forward - Prospective
Procedure
Who is being recruted

Arthritis+3

+ Joint Diseases

+ Musculoskeletal Diseases

Over 20 Years
+25 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: July 2023
See protocol details

Summary

Principal SponsorNational Taiwan University Hospital
Study ContactKe-Vin Chang, MD, PhDMore contacts
Last updated: August 6, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: July 26, 2023

Actual date on which the first participant was enrolled.

Knee osteoarthritis is increasingly recognized as a whole-joint disease involving not only articular cartilage but also periarticular soft tissues, including the cruciate and collateral ligaments. Although ultrasound elastography has been widely applied to musculoskeletal tissues, normative biomechanical data for knee ligaments remain limited, and the influence of osteoarthritis on ligament stiffness has not been fully characterized. The primary objective of this study is to establish normative shear wave elastography values for the ACL, PCL, MCL, and LCL across different age groups and ethnic populations and to determine their associations with demographic characteristics, body composition, and limb dominance. A secondary objective is to compare ligament stiffness between healthy individuals and patients with radiographic knee osteoarthritis. Participants will undergo standardized ultrasound examinations, SWE measurements, physical examinations, pain assessment using the Visual Analog Scale (VAS), and functional assessment using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). Patients with symptomatic knee osteoarthritis will initially receive conservative treatment according to routine clinical practice. Those who subsequently undergo clinically indicated ultrasound-guided injection therapy, including corticosteroid, hypertonic dextrose prolotherapy, or platelet-rich plasma (PRP), will receive repeat clinical and SWE evaluations after completion of treatment to investigate longitudinal changes in ligament biomechanical properties. The study will also assess measurement reliability through intra- and inter-rater analyses.

Principal SponsorNational Taiwan University Hospital
Study ContactKe-Vin Chang, MD, PhDMore contacts
Last updated: August 6, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

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

208 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 20 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

ArthritisJoint DiseasesMusculoskeletal DiseasesOsteoarthritisRheumatic DiseasesOsteoarthritis, Knee

Criteria

14 inclusion criteria required to participate
Able to ambulate independently without walking aids

Able to understand the study procedures and provide written informed consent

Able to understand the study procedures and provide written informed consent

Adults aged 20 years or older

Show More Criteria

11 exclusion criteria prevent from participating
Corticosteroid injection into the affected knee within the previous 3 months

Diagnosis of knee osteoarthritis within the previous 6 months

Healthy volunteers

Major knee or periarticular trauma

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

3 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

National Taiwan University Hospital, Bei-Hu Branch

Taipei, TaiwanOpen National Taiwan University Hospital, Bei-Hu Branch in Google Maps
Recruiting
One Study Center