- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg 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).
Studieoversigt
Status
Betingelser
Detaljeret beskrivelse
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.
Undersøgelsestype
Tilmelding (Anslået)
Kontakter og lokationer
Studiekontakt
- Navn: Sara Zacchetti
- Telefonnummer: 0039 0283502227
- E-mail: sara.zacchetti@grupposandonato.it
Undersøgelse Kontakt Backup
- Navn: Laura Mangiavini
- Telefonnummer: 0039 0283502227
Studiesteder
-
-
-
Milan, Italien, 20148
- Afsluttet
- Istituto Clinico San Siro
-
Milan, Italien, 20157
- Rekruttering
- IRCCS Ospedale Galeazzi-Sant'Ambrogio [coordinator]
-
Kontakt:
- Zacchetti
- Telefonnummer: 0039 0283502227
- E-mail: sara.zacchetti@grupposandonato.it
-
Torino, Italien, 10152
- Afsluttet
- Ospedale Cottolengo
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Prøveudtagningsmetode
Studiebefolkning
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.
Beskrivelse
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)
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
|---|
|
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
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Anterior Cortex Stylus
Tidsramme: 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.
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Results across study centres
Tidsramme: 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
Tidsramme: During surgery
|
Number of: adverse events, adverse device effects, serious adverse events and serious adverse device effects
|
During surgery
|
Samarbejdspartnere og efterforskere
Efterforskere
- Ledende efterforsker: Corrado Sosio, Ospedale Galeazzi S.p.A.
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- EMAX (L2055)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .