FH ORTHO SAS Knee Observatory

Knee Surgery Clinical Trial

Official title:

Post Market Clinical Follow-up of Knee Surgery Using FH ORTHO SAS Medical Devices (FH ORTHO SAS Knee Observatory)

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06207968
• Other study ID #: 2021-02
• Status: Not yet recruiting
• Start date: May 2024
• Est. completion date: June 2044

Study information

• Verified date: February 2024
• Source: FH ORTHO
• Contact: Cindy Lai
• Phone: 631315494
• Email: c.lai[@]fhortho.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The objective of this observatory is to generate additional real life clinical data in accordance with local regulation (i.e. Post-Market Clinical Follow-up (PMCF) study, a study carried out following the European Conformity (CE) marking of a device and intended to answer specific questions relating to clinical safety or performance (i.e. residual risks) of a device when used in accordance with its approved instructions for use (IFU).

The difficulty of such an observatory is to be able to collect data on the different versions of the devices, on the different possible combinations of implants of an knee arthroplasty. The observatory must also be able to cover devices used in ligament reconstruction surgery.

The observatory will be based on the principle of a "dynamic" cohort during the inclusion period, i.e. with possible inclusions to replace the premature exits.

Technical solutions will be implemented to facilitate data collection from surgeons (electronic Case Report Form (eCRF) and from patients (Electronic Patient Reported Outcome (ePRO) on smartphone/tablet/computer) when feasible.

The data to be collected and the different follow-up times are based on our state-of-the-art, clinical evaluation plans and clinical evaluation reports.

Description:

PMCF as part of CE mark renewal, to answer questions related to the safety and clinical performance of the devices, when used according to their approved instructions for use.

This is an European, prospective and retrospective, multicenter, non-comparative study.

Randomization is considered impossible due to surgeon preference, anatomical conditions and other patient factors, and the use of different techniques.

This observatory is non-comparative, due to the absence of a gold standard and the technical, logistical and contractual constraints involved.

This PMCF study (CE-marked MD, any class, used as intended) provide additional non-burdensome and non-invasive procedures.

The Observatory will therefore be based on the principle of a "dynamic" cohort, i.e. with possible exits and inclusions throughout the Observatory period.

The aim of this methodology is to have a sufficient number of patients to be able to carry out descriptive statistical analyses each year, and to be able to calculate the evaluation criteria with the longest possible follow-up of results. Data will be collected before surgery, during surgery and at follow-up visits. Data collection will focus on obtaining short- and long-term data for performance and safety evaluation (up to 20 years for knee arthroplasty prostheses; up to 5 years for knee ligament reconstruction devices). In the case of knee arthroplasty, it is recommended to have performance and safety data at 1, 2, 5 and 10 years of follow-up, as well as safety data at 15 and 20 years if possible. In the case of ligament reconstruction, it is recommended to have performance and safety data at 1 and 2 years, as well as safety data at 5 years. The platform will be able to send automatic notifications to surgeons to remind them of scheduled patient follow-ups, missing data, and encourage them to include new patients if necessary. Self-questionnaires will be completed by patients via a web-based platform, available on computer or smartphone/tablet. Alternatively, patients will complete paper self-questionnaires, which will then be entered into the database by the investigating team.

It will also be possible to arrange for direct telephone contact with patients by an independent structure guaranteeing non-dissemination of nominative data (e.g. CRO). Telephone contact can also be made if the patient is geographically remote or has difficulty travelling. Patient recruitment: Continuous, consecutive, prospective and retrospective (for some implants because few implants have been used for this condition) recruitment to guarantee a minimum number of patients per type of device. Individual written information for each patient will be mandatory. A signed patient consent form will be required in Europe, after sufficient time for reflection.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 487
• Est. completion date: June 2044
• Est. primary completion date: June 2044
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Any patient undergoing or having undergone implantation of medical devices distributed by FH ORTHO SAS for knee arthroplasty and ligament reconstruction, used in accordance with their approved IFU, in one of the centers participating in the Observatory.

• Patient is at least 18 years old at the time of surgery

• Patient agreeing to participate after having been informed orally and in writing (with written consent if required locally)

• In some countries, such as France, the patient will have to be socially insured to be included in the study.

Exclusion Criteria:

For Arthroplasty:

1. Infection, or latent infection

2. A mental or neuromuscular disorder that might create an unacceptable risk of instability, prosthetic fixation failure, or complications after surgery

3. Insufficient bone stock for proper implant fixation

4. It is the surgeon's responsibility to make sure that the patient does not have any known allergies to one of the compounds of the material listed on the product label.

5. Metabolic diseases that might compromise bone regrowth

6. Drug addiction

7. Incomplete bone growth

For Ligament reconstruction:

1. Infection, or latent infection

2. A mental or neuromuscular disorder that might create an unacceptable risk of instability, prosthetic fixation failure, or complications after surgery

3. Insufficient bone stock

4. Known allergies to one of the compounds of the material listed on the product label.

5. Metabolic diseases that might compromise bone regrowth

6. Uncooperative patient unable to follow recommendations

As the medical devices are used in real life according to their indications, pregnant or breastfeeding women are not excluded from the study, but for safety reasons it is not advisable to include them in the study.

Related Conditions & MeSH terms

• Knee Surgery

Intervention

Device:
• Knee surgery with FH Ortho devices
This clinical investigation is a real-life observatory designed to collect long-term clinical data on patients who have undergone knee joint replacement or knee ligament reconstruction. In this type of intervention, one or more medical devices distributed by FH ORTHO SAS may be used by surgeons.

Locations

Country	Name	City	State
France	Clinique De La Chataigneraie	Beaumont
France	Clinique De La Miotte	Belfort
France	Polyclinique St Privat	Boujan-sur-Libron
France	Clinique Du Val D'Ouest	Ecully
France	C.H. Raymond Poincare	Garches
France	Hôpital Saint Vincent de Paul	Lille
France	Hôpital Prive St Grégoire	Saint Gregoire
France	Polyclinique De L'Europe	Saint-Nazaire
France	Medipole Garonne	Toulouse
France	Hôpital Privé Océane	Vannes

Sponsors (1)

Lead Sponsor	Collaborator
FH ORTHO

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Patient satisfaction	A simple questionnaire consisting of 3 questions will be proposed to the patient. The 2 first one will be to graduate the satisfaction regarding the mobility and the pain of the operated knee and the last one is the yes/No question regarding the surgery reiteration.	3-6months, 1 year, 2 years, 5 years, 10 years
Other	X-ray	check the position of the prosthesis using medical imaging. Desired position: Yes or No	3-6months
Primary	Revision rate	Evaluate the revision rate at the longest follow-up possible for arthroplasty arm	2 months, 3-6 months, 1 year, 2 years, 5 years, 10 years, 15 years, 20 years
Primary	Revision rate	Evaluate the revision rate at the longest follow-up possible for ligament reconstruction arm	2 months, 3-6 months, 1 year, 2 years, 5 years
Secondary	International Knee Society (IKS 2011) score	Mobility, Pain and Function for Arthroplasty arm.; It includes a 100-point objective score and a subjective score made up of 3 domains evaluating satisfaction on 40 points, patient expectations on 15 points using different items between the pre- and post-operative phases, as well as functional activities on 100 points. The total score was 255 points. There are no levels and the results are expressed as raw scores. Higher scores mean a better outcome.	Pre-operative, 3-6months, 1 year, 2 years, 5 years, 10 years
Secondary	Complications/Adverse events	any adverse events leading or not to re-intervention (with or without change of the implant), including device malfunctions	During surgery, Immediate (0-2months), 3-6months, 1 year, 2 years, 5 years, 10 years
Secondary	International Knee Documentation Committee (IKDC 2000) score	Mobility, Pain and Function for Ligament Reconstruction arm; This self-questionnaire is divided into three parts (symptoms, sporting activities, function) and gives a score between 0 (worst) and 100 (best). This score is interpreted as a measure of functional capacity, with the highest scores representing the best levels of function and the lowest levels representing symptoms. A score of 100 means that there are no limits to daily activities and sports and that symptoms are non-existent.	Pre-operative, 1 year, 2 years
Secondary	Lysholm Knee Scoring Scale	Mobility, Pain and Function for Ligament Reconstruction arm The Lysholm Knee Score is a questionnaire that the patient completes with the therapist. The questionnaire is designed to assess the degree of knee instability, in terms of both impairment and limitation.; The Lysholm Knee Score calculates and rates an overall score from 0 to 100 based on 8 domains: squatting, locking, pain, stair climbing, weight bearing, instability and oedema. Doctors use this condition-specific subjective outcome score to assess a patient's progress after knee surgery or injury. Scores between 95 and 100 are considered exceptional, those between 84 and 94 acceptable, those between 65 and 83 fair and those below 65 poor.	Pre-operative, 1 year, 2 years
Secondary	Tegner activity level scale	Mobility, Pain and Function for Ligament Reconstruction arm; The Tegner activity scale is a numerical scale with values ranging from 0 to 10, each representing a different activity. A person is considered to have an activity level of 10 if they play highly competitive sports such as rugby, football and soccer. A person who plays the above sports recreationally is considered to have an activity level of 6. A person with knee problems who is on sick leave or receiving a disability pension is considered to have an activity level of 0.	Pre-operative, 1 year, 2 years
Secondary	Knee laxity (clinical section)	Mobility, Pain and Function for Ligament Reconstruction arm.; This questionnaire is completed by the physician. He will assessed laxity of operated knee, as: Pivot Shift test: absent (0), grade 1 (+), grade 2 (++), grade 3 (+++).	Pre-operative, 3-6 months
Secondary	Complications/Adverse events	Any adverse events leading or not to re-intervention (with or without change of the implant), including device malfunctions	During surgery, Immediate (0-2months), 3-6months, 1 year, 2 years, 5 years
Secondary	Visual Analogue Scale (VAS)	for arthroplasty arm Pain rating scale. A straight horizontal line of fixed length, usually 100 mm. The ends are defined as the extreme limits of the pain to be measured orientated from the left (worst) to the right (best).; The scale is given to the patient during the consultation, the patient indicates his/her level of pain and the surgeon then transcribes the score.	1 year, 2 years, 5 years, 10 years, 15 years, 20 years
Secondary	Visual Analogue Scale (VAS)	for ligament reconstruction arm Pain rating scale. A straight horizontal line of fixed length, usually 100 mm. The ends are defined as the extreme limits of the pain to be measured orientated from the left (worst) to the right (best).; The scale is given to the patient during the consultation, the patient indicates his/her level of pain and the surgeon then transcribes the score.	1 year, 2 years, 5 years
Secondary	ASA (American Society of Anesthesiologists)-score	The American Society of Anesthesiologists proposes five classes of patients requiring anaesthesia.; Class 1: patient in good health. Class 2: patient with moderate general illness. Class 3: patient with a serious but not incapacitating general illness. Class 4: patient with a life-threatening general illness. Class 5: a moribund patient who would not survive 24 hours without the procedure, the outcome of which is uncertain.	Pre-operative