Medacta NextAR TKA Pivotal Trial

Not Applicable

Completed

• Conditions: Musculoskeletal Diseases
• Interventions: Device: NextAR TKA system

• Registration Number: NCT04844879
• Lead Sponsor: Medacta International SA

Brief Summary

The goal of this study is to assess the efficacy and safety of a navigation system providing personalized soft tissue balance data in medially-stabilized total knee arthroplasty (TKA).

Detailed Description

This is a prospective, multicentre, single-arm, open, confirmatory clinical investigation to assess the efficacy and safety of a navigation system providing personalized soft tissue balance data in medially-stabilized total knee arthroplasty (TKA).

Participants will be informed about the study, both orally and in writing, during a preoperative visit. The investigator will answer any questions that may arise and will collect the informed consent. During the study, enrolled participants will be able to withdraw at any time and for any reason.

The study is conducted according to the following schedule:

* V1 : Inclusion during a preoperative visit

* V2: Surgery

* V3: Follow-up visit at 2 month post-surgery

* V4: Follow-up visit at 6 months post-surgery

* V5: Follow-up visit at 12 months post-surgery

The following data will be collected:

* Oxford Knee Score (OKS), Knee Society Score (KSS), Forgotten Joint Score (FJS) and patient satisfaction at 6 months and 12 months of follow-up;

* Radiological analysis at 2 and 12 months of follow-up;

* Surgical time (min);

* Necessity of soft tissue release to obtain ligament or patellar balance;

* Time to discharge (days);

* Device deficiencies and peri- and postoperative adverse events.

A web-based data collection tool will be used as Electronic Data Capture (EDC). All the information required by the protocol will be collected in electronic case report forms (eCRF).

The statistical analysis will be performed according to a pre-established statistical analysis plan. Missing values will not be replaced by estimated values but will be considered as missing in the statistical analysis.

Study Timeline

• Study First Submitted: 2021-04-08
• Study First Submitted QC: 2021-04-12
• Study First Posted: 2021-04-14
• Study Start: 2021-05-17
• Primary Completion: 2023-12-31
• Study Completion: 2024-06-18
• Status Verified: 2024-11
• Last Update Submitted: 2024-11-19
• Last Update Posted: 2024-11-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

1. Males and females aged over 18 years at time of surgery.
2. Patients who are scheduled to receive Medacta GMK® Sphere system for primary TKA (class III, CE-marked).
3. Patients with functional contralateral knee (i.e. without the need to use walking aids).
4. Patients willing and able to provide written informed consent for participation.
5. Patients willing to comply with the pre and post-operative evaluation schedule.

Exclusion Criteria

1. Patients with one or more medical conditions identified as a contraindication defined by the labelling on any Medacta implants used in this study:

   • Patients presenting with progressive local or systemic infection
   • Muscular loss, neuromuscular disease or vascular deficiency of the affected limb, making the operation unjustifiable.
   • Severe instability secondary to advanced destruction of condralar structures or loss of integrity of the medial or lateral ligament

2. Patients whose prospects for a recovery to independent mobility would be compromised by known coexistent, medical problems.

3. Patients affected by concomitant spine, hip, ankle or contralateral knee pathologies that can affect walking capacity.

4. Patients unable to understand and take action.

5. Patients with known allergy to the materials used.

6. Patients in which Medacta GMK® Sphere system is used in emergency interventions.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Single-arm	NextAR TKA system	Patients suitable to receive Medacta GMK® Sphere system for primary TKA will be invited to take part to the study during the preoperative visit. Follow-ups are performed after 2, 6 and 12 months. Data collection includes clinical and radiological data for preoperative and postoperative assessments, as well as intraoperative details.

Primary Outcome Measures

Name	Time	Method
Functional outcome	6 months	Oxford Knee Score (OKS)

Secondary Outcome Measures

Name	Time	Method
Clinical and functional outcome	6 months and 12 months	Knee Society Score (KSS)
Surgical outcome - Surgical time	Intraoperative	Surgical time (min)
Surgical outcome -Time to discharge	2 months	Time to discharge (days)
Surgical outcome - Necessity of soft tissue release	Intraoperative	Necessity of soft tissue release to obtain ligament or patellar balance (Y/N)
Functional outcome	6 months and 12 months	Forgotten Joint Score (FJS)
Radiological outcomes	2 months and 12 months	Radiological assessment including implant positioning, presence of radiolucent lines, subsidence, migration of components, presence of heterotopic ossifications or osteolysis
Safety outcomes	Intraoperative, 2 months, 6 months and 12 months	Device deficiencies and adverse events

Trial Locations

Locations (4)

Privatklinik Belair; 🇨🇭 Schaffhausen, Switzerland

Uniklinik Balgrist; 🇨🇭 Zurich, Switzerland

Privatklinik Lindberg; 🇨🇭 Winterthur, Switzerland

Kantonsspital Winterthur; 🇨🇭 Winterthur, Switzerland