Skip to main content
Clinical Trials/NCT04682496
NCT04682496
Completed
Not Applicable

Evaluation of the Influence of Ultrasound Probe Pressure on the Intratendon Doppler Signal in Patellar Tendinopathy

Cardenal Herrera University1 site in 1 country30 target enrollmentDecember 18, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Patellar Tendinitis
Sponsor
Cardenal Herrera University
Enrollment
30
Locations
1
Primary Endpoint
number of signals (n)
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

In the sports field, patellar tendinopathy is, as a pathology, one of the main concerns for athletes, both because of its incidence and because of the difficulty involved in their recovery. At the ultrasound level, tendinopathies can be divided, depending on the presence or absence of an intratendon Doppler signal, into hypervascular or hypovascular tendinopathy. Its classification is, today and clinically speaking, merely qualitative through the observation of the explorer. The ultrasound evaluation is carried out through a probe that is placed on the patient's skin, the procedure to be followed to obtain a vascular image is merely operator-dependent, that is, the position of the probe, the pressure exerted on the skin or even ultrasound optimization parameters can drastically modify the results.

Due to high pressure on the probe, the intratendon Doppler signal may be diminished in the quantitative variables of area, number of signals, pixel intensity, perimeter, solidity, perfusion index, circularity, major and minor diameter.

From a certain pressure on the probe, the intratendon Doppler signal can be drastically altered.

This study will try to evaluate the influence of the pressure exerted by the examiner with the probe on the quantitative variables of the intratendon Doppler signal in patellar tendinopathy.

To carry out the study, a single group with patellar tendinopathy will be established. Ultrasound evaluations with Doppler mode will be performed on the tendon using different probe pressures, monitoring the applied force and recording the images obtained for later analysis.

Registry
clinicaltrials.gov
Start Date
December 18, 2020
End Date
February 7, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Cardenal Herrera University
Responsible Party
Principal Investigator
Principal Investigator

SERGIO MONTERO NAVARRO

Principal Investigator

Cardenal Herrera University

Eligibility Criteria

Inclusion Criteria

  • Acceptance of participation in the study.
  • Diagnosis of patellar tendinopathy with the presence of an intratendon Doppler signal.
  • Subjects between the ages of 18 and 65.

Exclusion Criteria

  • Present some type of surgical intervention in the region to be explored that could alter in some way the ultrasound evaluation.
  • Refer vascular pathology or the intake of medication that may alter blood flow or density.
  • Having been treated with sclerosing techniques that can alter the perfusion or vascular resistance of the tendon tissue.

Outcomes

Primary Outcomes

number of signals (n)

Time Frame: during intervention

number of intratendon doppler signals (unit)

Perimeter (mm)

Time Frame: during intervention

perimeter of the intratendon Doopler signal (mm)

Solidity

Time Frame: during intervention

measures the density of an object (0-1 Units on a scale)

Resistance index

Time Frame: during intervention

resistance index of intratendon Doppler signals (0-1 Units on a scale)

Force

Time Frame: during intervention

force applied by the probe on the knee during the scan (N)

major diameter (mm)

Time Frame: during intervention

major diameter of the intratendon Doppler signal (mm)

Area (mm^2)

Time Frame: during intervention

intratendon Doppler signal area (mm\^2)

Average pixel intensity (0-255 Units on a scale)

Time Frame: during intervention

average pixel color intensity (0-255 Units on a scale)

minor diameter (mm)

Time Frame: during intervention

minor diameter of the intratendon Doppler signal (mm)

Circularity

Time Frame: during intervention

measure of roundness or circularity, area-to perimeter ratio. (0-1 Units on a scale)

Secondary Outcomes

  • Age (years)(Post-intervention)
  • Time of evolution (months)(months)
  • Pain location(Immediately pre-intervention)
  • hours of training (hours)(Immediately pre-intervention)
  • Dominance(post-intervention)
  • Victorian Institute of Sport Assessment-Patella (VISA-P)(Immediately pre-intervention)
  • Time without training (months)(Immediately pre-intervention)
  • Sex (female or male)(post-intervention)

Study Sites (1)

Loading locations...

Similar Trials