Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
NCT06809920

Analysis Of Knee Joint Of Patients With Anterior Cruciate Ligament Injury Undergoing Physiotherapy After Two Different Surgical Techniques: A Randomized Clinical Trial.

Led by Universidade Estadual de Londrina · Updated on 2026-05-08

20

Participants Needed

3

Research Sites

147 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The objetive is compare knee joint stability, functional capacity, postural control, activation, and muscle strength of patients undergoing conventional Anterior Cruciate Ligament Reconstruction or the conventional Anterior Cruciate Ligament Reconstruction + Anterolateral Ligament Reconstruction technique of the knee, and rehabilitation for up to nine months. This project aims to include patients with ACL injuries already treated at the Knee Outpatient Clinic of the Hospital das Clínicas da UEL (HC-UEL), coordinated by the orthopedic physician Dr. Lucas da Fonseca Borghi, who has his master's degree related to this research project. Twenty patients between 18 and 50 years old, of both sexes, sedentary and/or active and/or athletes, diagnosed with unilateral injury of the Anterior Cruciate Ligament will be included. These patients will be evaluated, submitted to ACL surgery (conservative) or associated with ALL reconstruction and undergo rehabilitation with physiotherapy in conjunction with the extension project Sports Physiotherapy from Theory to Practice - Phase III (PROEX-UEL No 02675), coordinated by Prof. Dr. Christiane S. Guerino Macedo - advisor of this research. Expected results: It is expected that the group undergoing ACL + ALL reconstruction will present better knee joint stability, functional capacity, postural control, activation and muscle strength.

CONDITIONS

Official Title

Analysis Of Knee Joint Of Patients With Anterior Cruciate Ligament Injury Undergoing Physiotherapy After Two Different Surgical Techniques: A Randomized Clinical Trial.

Who Can Participate

Age: 18Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants aged 18 to 50 years
  • Both sexes
  • Sedentary, active, or athletes
  • Diagnosed with unilateral ACL injury
  • Reside in the city of Londrina - PR
Not Eligible

You will not qualify if you...

  • Body mass index (BMI) above 35 kg/m2
  • Multidirectional ligament laxity
  • Associated multiligament injury (PCL and posterolateral corner)
  • Previous or current lower limb fractures
  • Previous ACL reconstruction (revision)
  • Signs of osteoarthritis
  • Indication for meniscus suture
  • Neurological disease
  • Pregnant women
  • Heart disease
  • Previous lower limb surgeries

AI-Screening

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Trial Site Locations

Total: 3 locations

1

university hospital of the State University of Londrina

Londrina, Paraná, Brazil, 86038-350

Actively Recruiting

2

University Hospital of the State University of Londrina

Londrina, Paraná, Brazil, 86038-350

Actively Recruiting

3

State University of Londrina

Londrina, Paraná, Brazil, 86041-263

Actively Recruiting

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Research Team

C

Christiane Macedo

CONTACT

C

Caroline de Camargo

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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