Retrospective Study on Clinical Performance and Safety Profile of Agile Nail

NCT ID: NCT06412939

Last Updated: 2025-08-28

Basic Information

• Recruitment Status: TERMINATED
• Total Enrollment: 20 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2024-07-26
• Study Completion Date: 2025-03-26

Brief Summary

This study aims to retrospectively collect data from routine clinical practice in order to evaluate the safety profile of the Agile intramedullary nail, used in pediatric patients according to the manufacturer Instructions For Use (IFU) in the time frame from the time of surgery until the last follow-up visit available at the hospitals.

Detailed Description

The study will be conducted in two investigational sites, one in France and one in United Kingdom, both experienced in the treatment of pediatric patients with femoral shaft and subtrochanteric fractures and deformity correction procedures or have performed prophylactic nailing of impending pathologic fractures, where the usage of AGILE NAIL (known as AGILE) was part of the normal clinical practice.

Investigator of both study sites will provide data for a maximum of 45 patients meeting inclusion and exclusion criteria (Considering a drop-out or a non-evaluable rate of 10% of the procedures) that will contribute for approximately 45 procedures in which AGILE was used.

No diagnostic or therapeutic intervention outside of routine clinical practice will be applied. The study has been designed to analyze medical records of patients where study data was collected as part of their routine clinical practice. Therefore, patients will be retrospectively enrolled in the study. Patients who have undergone AGILE implantation from 04/2018 to 12/2022 are considered for the study. The observation period of study subjects will comprise from surgery until the last follow up visit available.

Medical records of the participating sites are expected to contain all the required information.

In United Kingdom, no study visit will be required but according to local legislation, it will be essential that before collecting any information from medical records, participants or their guardians are asked for specific informed consent to be signed by them before any collection of patient information takes place.

However, in France, due to the use of primary data and the foreseen exemption of the informed consent (IC) form (see Section 14.2 Informed Consent), no study visit will be required.

Conditions

Fractures, Bone; Impending Fracture; Deformity; Bone

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: RETROSPECTIVE

Study Groups

Patients in pediatric age (> 18 month and < 18 years) at the time of surgery

The full analysis set includes all paediatric patients who that have been treated for femoral shaft and subtrochanteric fractures or have performed prophylactic nailing of impending pathologic fractures or have undergone fixation of femurs that have been surgically prepared for deformity correction with the Agile nail, that will be systematically consecutive screened at the centers.

Agile Nail

Intervention Type: DEVICE

Intramedullary implantation of the Agile intramedullary rigid nail in femur to provide bone fixation

Interventions

Agile Nail

Intramedullary implantation of the Agile intramedullary rigid nail in femur to provide bone fixation

Intervention Type: DEVICE

Other Intervention Names

Rigid intramedullary nail

Eligibility Criteria

Inclusion Criteria

1. The patient has been adequately informed by providing the PIS. 1.1 The patient expressed his willingness to participate in the Study by signing and dating informed consent (valid only for UK patients according to local law).

2. Patients who had a regular indication for surgical intervention with Agile Nail according to the manufacturer's IFU.

3. Patients in pediatric age ((> 18 month and < 18 years) at the time of surgery.

4. Patients skeletally immature.

5. Patients who underwent surgery performed with Agile Nail.

6. Patients with clinical data registered in her/him medical records sufficient to assess the safety and efficacy endpoint of the study: in particular, the patient has at least one followup at minimum 3 months from the surgery where is possible for the investigator to assess the consolidation of the treated bone.

7. The patient had surgery at least 1 year before enrollment.

Exclusion Criteria

1. Patient who had/has a medical condition that is a contraindication according to the manufacturer's instruction for use leaflet.

2. Patient who had/has a concomitant not permitted device which cannot be safely removed.

3. Patient for whom there are other concurrent medical or other conditions that in the opinion of the participating investigator may prevent participation or otherwise render the patient ineligible for the study.

4. The patient had surgery less than 1 year before enrollment.

• Minimum Eligible Age: 18 Months
• Maximum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Orthofix s.r.l.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Patrick Foster, MD

Role: PRINCIPAL_INVESTIGATOR

Leeds Teaching Hospitals NHS Trust

Locations

Leeds Teaching Hospitals NHS Trust

Leeds, , United Kingdom

Countries

United Kingdom

Other Identifiers

335551

Identifier Type: OTHER

Identifier Source: secondary_id

OCI_2304

Identifier Type: -

Identifier Source: org_study_id