Detail Article

Informations générales (source: ClinicalTrials.gov)

Numéro NCT

NCT06156384 En recrutement

Titre

Prospective, Observational Study to Assess the Pain, Satisfaction, and Quality of Life of Patients Implanted With the FITBONE® Lengthening Nail (FitForFrance)

Type

Observational

Pathologie

Inégalité de longueur des membres inférieurs

Phase

Promoteur

Orthofix s.r.l. (Voir sur ClinicalTrials)

Date de début

juin 2024

Date de fin

juin 2028

Dernière mise à jour

05 avril 2025

Résumé

This study is a prospective observational non-interventional multi-centre cohort study of patients, 12 years or older, initiating a lower limb lengthening procedure with FITBONE and who have a length discrepancy of 30mm or more between the limbs. The following parameters will be assessed for up to 24 months. - Pain using the Visual Analog Scale (VAS), Patient Global Assessment (PGA) and Clinical Observer Global Assessment (COGA) - Patient satisfaction using the Patient Global Impression of change (PGI-C) scale - QoL using the 36-Item Short Form Survey/Paediatric Quality of Life Inventory (SF-36/PedsQL)

Détail

Voir le détail The study period is 24 months post-surgery. Each patient's demographic data, medical history, any relevant concomitant medication, physical examination, range of motion data will be recorded using a standardized case record form after informed consent is provided and the healthcare provider completes a physical examination regarding the patient's conditions and record determination as to whether FITBONE is recommended. The decision to treat, observe, and to include in this observation study is at the discretion of the healthcare provider. This is an observational study and therefore, the participating healthcare provider will manage patients according to the usual clinical practice. Surgery will be performed according to the standard surgical procedure described previously. Study of Investigational Product(s). Five to ten days after the lengthening nail placement, the lengthening mechanism is operated by transmitting energy necessary for the lengthening from the outside. This period is referred to as the distraction period. The rhythm of lengthening and strict protocol for an individual patient, indicating the daily lengths of lengthening to be applied, are decided by the healthcare provider taking into account all influencing factors. Therefore, the end of the distraction period, bone healing, implant removal, and 6 months post-implant removal may differ by individual. In the event the distraction period is extended by the healthcare provider, the new distraction period will determine the end of the distraction time point. All patients will be followed until the end of the scheduled study period regardless of any change in their treatment or other conditions. Six visits are planned: 1. Surgery (baseline) 2. End of the distraction phase 3. End of bone healing 4. Implant removal 5. 6-month post-removal 6. 24-month post-surgery The satisfaction will be assessed at implant removal, 6 months post implant removal, and 24 months post-surgery. The QoL will be assessed at baseline, at 6 months post implant removal, and 24 months post-surgery. Pain will be assessed at all timepoints. Measurement of pain at the end of the distraction phase, the patient will be requested to report the pain experienced in the past week, at the moment, and during or immediately after the distraction period. At other time points, pain for only at the moment will be captured. Range of motion (ROM) will be measured at the end of bone healing, and at the 24 months post-surgery. Lengthening achieved will be measured at the end of bone healing. Any incidence of adverse events will be recorded at any point during the 24-month follow-up period. Fermer le détail

Etablissements

Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
Centre hospitalier universitaire (CHU) de Toulouse - 31300 - Toulouse - Occitanie - France	Franck Accadbled, Prof.	En recrutement	Contact (sur clinicalTrials)
CHU de Saint-Étienne Hôpital Nord - 42270 - Saint-Étienne - Auvergne-Rhône-Alpes - France	Hassan Al Khoury Salem, MD	En recrutement	Contact (sur clinicalTrials)
CHU de Strasbourg - 67091 - Strasbourg - Grand Est - France	Ludovic Paul Schneider, MD	En recrutement	Contact (sur clinicalTrials)
CHU Lille - Hôpital Jeanne de Flandre - 59120 - Lille - Hauts-de-France - France	Damien Fron, MD	En recrutement	Contact (sur clinicalTrials)
Hôpital Sainte-Marguerite AP-HM - 13274 - Marseille - Provence-Alpes-Côte d'Azur - France	Maxime Fabre-Aubrespy, MD	En recrutement	Contact (sur clinicalTrials)

Critères

Genre

Tous

Nombre d'inclusion

Critère d'inclusion

Inclusion Criteria:

- Patients aged ≥12 years old, with congenital or acquired lower limb discrepancy
greater than 30mm, undergoing femoral or tibia bone lengthening with FITBONE

- Patients with a regular indication for a surgical intervention with FITBONE
according to manufacturer IFU

- The patient (or his/her legally acceptable representative) is capable of
understanding the content of the Informed Consent Form (ICF)

- The informed consent form is correctly obtained

Critère de non inclusion

- Patients with a medical condition that is contraindicated according to the FITBONE
instruction for use.

- Patients with any conditions that, in the Investigator's opinion, may interfere with
the study execution, including those likely to be lost to follow-up.

- Patients who have any conditions or medical condition that, in the investigator's
opinion, may interfere with the study's execution or in which the patient should not
participate for safety reasons.

- Patients requiring the application of or have already in-situ concomitant devices
that cannot be safely removed (except for permitted concomitant devices).

- Patients participating in other clinical or have taken part in any clinical study in
the last 3 months.

NCT06156384 - Prospective, Observational Study to Assess the Pain, Satisfaction, and Quality of Life of Patients Implanted With the FITBONE® Lengthening Nail (FitForFrance)

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Etablissements
Critères
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