- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07815080
Femoral Component TKA: Extramedullary vs Conventional Intramedullary Guide (EMAX (L2055))
Positioning Femoral Component TKA Using an Extramedullary Guide: Comparison With Conventional Intramedullary Guide
The study wants to evaluate the performance of this EM guide in comparison to a traditional IM guide.
75 patients will be included in the extramedullary group (to be compared with a corresponding previous group of 75 patients treated with intramedullary guide).
Aperçu de l'étude
Statut
Les conditions
Description détaillée
Total Knee Arthroplasty (TKA) is a widely performed surgical procedure aimed at relieving pain and restoring function in patients with advanced knee arthritis. The success of TKA is contingent upon precise implant positioning, particularly in relation to the femoral component. The femoral component's alignment significantly influences postoperative knee biomechanics, patient satisfaction, and long-term implant survival.
Conventional methods for femoral component positioning involve the use of intramedullary (IM) guides, which are inserted into the femoral canal to align the cutting block for bone preparation. While IM guides offer precise alignment, they can also lead to complications such as intraoperative fractures, fat embolism, activation of coagulation and excessive blood loss.
To address these limitations, extramedullary (EM) guides have emerged as an alternative option. EM guides are placed on the external surface of the femur without entering the medullary canal and avoiding complications that may occur reaming the canal.
In the recent past years, kinematic alignment (KA) has become widespread in use as a new technique for TKR that considers the patient's individual alignment and biomechanics. By restoring the pre-arthritic kinematic axes of the femur and tibia, KA aims to mimic the natural knee joint's function and movement.
In this study a specific EM guide - Anterior Cortex Stylus - is used to address the alignment of the femoral component in the context of a KA approach. The guide uses the anterior cortex of the distal femur as reference for cutting block positioning. The study aims to evaluate the performance of this EM guide in comparison to a traditional IM guide (used in previous group of patients).
This is an open, multi-centre, retro-prospective, observational, controlled study.
The primary aim is to evaluate whether the Anterior Cortex Stylus (in a retro-prospective collected series) is not inferior to the traditional intramedullary guide (previous group of patients) in term of positioning of the femoral component in TKA.
A total of 75 patients will be included in the extramedullary group (to be compared with a corresponding previous group of 75 patients treated with intramedullary guide). Both groups will be treated with a total knee arthroplasty using GMK Sphere (CE marked, class III) and a kinematic alignment approach.
Type d'étude
Inscription (Estimé)
Contacts et emplacements
Coordonnées de l'étude
- Nom: Sara Zacchetti
- Numéro de téléphone: 0039 0283502227
- E-mail: sara.zacchetti@grupposandonato.it
Sauvegarde des contacts de l'étude
- Nom: Laura Mangiavini
- Numéro de téléphone: 0039 0283502227
Lieux d'étude
-
-
-
Milan, Italie, 20148
- Complété
- Istituto Clinico San Siro
-
Milan, Italie, 20157
- Recrutement
- IRCCS Ospedale Galeazzi-Sant'Ambrogio [coordinator]
-
Contact:
- Zacchetti
- Numéro de téléphone: 0039 0283502227
- E-mail: sara.zacchetti@grupposandonato.it
-
Torino, Italie, 10152
- Complété
- Ospedale Cottolengo
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Méthode d'échantillonnage
Population étudiée
The study shall include a total of 150 patients: 75 will be included in the extramedullary group, to be compared with a corresponding previous group of 75 patients treated with intramedullary guide. Patients meeting the inclusion criteria (mentioned below) will be recruited separately by each participating institution.
Patient enrolled in the retrospective analysis have been operated upon between January 2021 and September 2025.
La description
Inclusion Criteria:
- Male or female ≥ 18 years old
- Indication to primary TKA, for any diagnosis operated with EM or IM guides
- Signature of the informed consent (only for prospective cohort)
- Been operated upon between January 2021 and September 2025 (only for retrospective cohort)
Exclusion Criteria:
- Revision surgery of knee arthroplasty
- Patients with malignant diseases (at the time of surgery)
- Patients with proven or suspect infections (at the time of surgery)
- Pregnancy end/or lactating (auto declaration)
- Patient with known allergy to the specific metallic components of the prosthesis (at the time of surgery)
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
|---|
|
Extramedullary (EM) guides: Retroprospective + Prospective cohort
patients trated with extramedullary (EM) guides.
This cohort can be both Retroprospective and Prospective
|
|
intramedullary (IM) guides: Retrospective cohort
patients trated with intramedullary (IM) guides.
This cohort will be only Retrospective
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Anterior Cortex Stylus
Délai: Radiographic angle at 3 moth post-op in the sagittal plane, between the anterior cortex of the distal femur and the femoral component and compare it in the group operated with Anterior Cortex Stylus versus the group operated with IM guide.
|
Radiographic angle at 3 moth post-op of the femoral component in TKA in an Anterior Cortex Stylus (retro-prospective collected series) compared to intramedullary guide (previous group of patients)
|
Radiographic angle at 3 moth post-op in the sagittal plane, between the anterior cortex of the distal femur and the femoral component and compare it in the group operated with Anterior Cortex Stylus versus the group operated with IM guide.
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Results across study centres
Délai: Compare the results in terms of radiographic sagittal angle between study centres at pre-op, surgery and 3 month post-op.
|
Radiographic angles compared between the centres (at pre-op, surgery and 3 month post-op)
|
Compare the results in terms of radiographic sagittal angle between study centres at pre-op, surgery and 3 month post-op.
|
|
Adverse Events to determinate Instrument safety
Délai: During surgery
|
Number of: adverse events, adverse device effects, serious adverse events and serious adverse device effects
|
During surgery
|
Collaborateurs et enquêteurs
Les enquêteurs
- Chercheur principal: Corrado Sosio, Ospedale Galeazzi S.p.A.
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- EMAX (L2055)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .