Novel Method for Diagnosing Lateral Patellar Compression Syndrome Using X-ray: a Retrospective Case-Control Study

Sponsor
Peking University Third Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04454593
Collaborator
(none)
87
1
2
43.4

Study Details

Study Description

Brief Summary

This study evaluates whether the patellar axial radiograph of lateral patellar curvature angle (LPCA)with knee flexion at 30 ° can be used as a new diagnostic surrogate of lateral patellar compression syndrome(LPCS). We believe that the new index LPCA has high sensitivity and specificity in initial diagnosis of LPCS using axial patellar radiograph with knee flexion at 30 ° , and has high application value.

Condition or Disease Intervention/Treatment Phase
  • Other: no intervention

Detailed Description

Background: A well-established reference is lacking for diagnosing lateral patellar compression syndrome (LPCS), and this diagnosis currently depends on clinicians' subjective judgment and several examination results. X-rays are primarily used to diagnose LPCS, but they have low detection rates of patellar tilt using the congruence angle (CA) and patellar tilting angle (PTA).

Purpose: To investigate whether patellar axial radiography of the lateral patellar curvature angle (LPCA) of knee in 30° flexion can diagnose LPCS.

Methods: We enrolled 87 patients between 2016 and 2019 and divided them as per diagnosis into three groups of 29 each: LPCS, patellar dislocation (PD, control), and meniscus tear (MT, negative control) groups. A senior radiologist and the chief physician of sports medicine examined their patellar axial radiographs of the knee in 30° flexion using a computer imaging system, measuring LPCA, PTA, and CA. Univariate analysis of variance and Kruskal-Wallis H test were used to compare measurement data with normal distribution and non-normal distribution, respectively. Bonferroni correction was used to analyze different indicators for different groups. The area under the curve (AUC) was calculated to verify the value of LPCA in initial diagnosis of LPCS.

Study Design

Study Type:
Observational
Actual Enrollment :
87 participants
Observational Model:
Case-Control
Time Perspective:
Retrospective
Official Title:
Novel Method for Diagnosing Lateral Patellar Compression Syndrome Using X-ray: a Retrospective Case-Control Study
Actual Study Start Date :
Mar 22, 2020
Actual Primary Completion Date :
Apr 22, 2020
Actual Study Completion Date :
May 22, 2020

Arms and Interventions

Arm Intervention/Treatment
Lateral patellar compression syndrome

Patients diagnosed with lateral patellar compression syndrome between February 2016 and April 2019

Other: no intervention
This is an observation study,with no intervention

patellar dislocation

Patients diagnosed with patellar dislocation between February 2016 and April 2019

Other: no intervention
This is an observation study,with no intervention

meniscus tear

Patients diagnosed with meniscus tear between February 2016 and April 2019

Other: no intervention
This is an observation study,with no intervention

Outcome Measures

Primary Outcome Measures

  1. lateral patellar curvature angle [between 2016 and 2019]

    lateral patellar curvature angle in three groups was compared

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients were diagnosed as LPCS ,MT and PD respectively
Exclusion Criteria:
  • patients with ligament injury, malunion of patella fracture, free bodies in the joint, surgical contraindications, and with both knees affected.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Peking University Third Hospital Beijing Beijing China 100191

Sponsors and Collaborators

  • Peking University Third Hospital

Investigators

  • Study Chair: Yang Yu-ping, Peking University Third Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Peking University Third Hospital
ClinicalTrials.gov Identifier:
NCT04454593
Other Study ID Numbers:
  • M2019464
First Posted:
Jul 1, 2020
Last Update Posted:
Jul 1, 2020
Last Verified:
Jun 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Peking University Third Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 1, 2020