ClinicalTrials.Veeva

Menu

Intraoperative Laxity Assessment of ACL Reconstruction, ACL Revision and MAT (INTRA_KIN)

I

Istituto Ortopedico Rizzoli

Status

Active, not recruiting

Conditions

Intraoperative Musculoskeletal Injury

Treatments

Procedure: ligament reconstruction and meniscus transplantation

Study type

Observational

Funder types

Other

Identifiers

NCT03441165
INTRA_KIN

Details and patient eligibility

About

Intraoperative knee laxity evaluation of patiente undergoing ACL reconstruction, ACL revision, MAT

Full description

The study aims to include all thise patients who will undergo anterior cruciate ligament reconstruction, anterior cruciate ligament revision or meniscus transplantation. These patients will undergo an intraoperative kinematic evaluation (pre- and post-ligament reconstruction / meniscal transplantation). There is no follow-up because all the data necessary to carry out the study are obtained during the operating session. In particular, the pre- and post-intervention values (acquired intraoperatively) will be compared using both the surgical navigator and the KiRA system in order to evaluate the effect of the surgical procedure on the value of both static and dynamic laxity of the knee joint. Moreover, limited to the data acquired with the KiRA system, a comparison will be also made with the controlateral limb.

Enrollment

500 patients

Sex

All

Ages

14 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients who have provided written informed written consent
  2. Patients aged 14 to 65
  3. Patients undergoing reconstructive surgery of the anterior cruciate ligament or revision of anterior cruciate ligament surgery or meniscus transplantation. Patients unable to understand and want patients who have not signed informed consent

Exclusion criteria

  1. Patients unable to understand and to want
  2. Patients who have not signed informed consent

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems