Skip to content

A Focused Registry on the Femoral Neck System (FNS) in Patients With Femoral Neck Fractures

A Focused Registry on the Femoral Neck System (FNS) in Patients With Femoral Neck Fractures

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02422355
Acronym
FR_FNS
Enrollment
125
Registered
2015-04-21
Start date
2017-09-30
Completion date
2021-12-31
Last updated
2023-01-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Femoral Neck Fracture, Hip Fracture

Keywords

hip, femoral neck, Garden classification, healing, cut-out, iatrogenic fracture, implant, rotational stability, minimal invasive

Brief summary

In comparison to previous implants, the Femoral neck system (FNS) is an approved implant by the competent authorities (CE mark). It is designated to stabilize medial femoral neck fractures in a minimal invasive technique. The implant combines an angular stable device with screw in screw technology for rotational stability. Therefore the purpose of this focused registry is to investigate how the newly developed and approved implant called FNS is performing clinically and radiologically in terms of surgical technique, intra- and postoperative complications and short term outcome.

Detailed description

All patients included are treated as per standard or care and followed up from the time point of enrollment until at least three months after surgery as described below. Data of a visit after 6 months and 12 months are collected if bone union according to the RUSH score is not complete after 3 or 6 months respectively or if the patient has persistent or increasing pain on the operated site. Preoperative: * Patient details * Fracture Classification and comminution based on CT * Pre-fracture HHS and EQ5D * X-rays Intraoperative: * Surgery details * Defined intraoperative complications * Intraoperative fluoroscopy: hip ap (with leg 15° internally rotated) and lateral after reduction and after implant placement Postoperative: * X-ray prior to any mechanical load: hip ap (with leg 15° internally rotated) and lateral 6 weeks and 3 months FU: * Defined postoperative complications * HSS and EQ5D * X-rays

Interventions

DEVICEFNS

Surgical intervention using the FNS

Sponsors

AO Innovation Translation Center
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 18 years and older * Diagnosis of a medial femoral neck fracture (AO/OTA 31-B1:3) with the need of a fixation using the FNS. * Ability to understand the content of the patient information/Informed Consent Form * Willingness and ability to participate in the registry according to the Registry Plan (RP) * Signed and dated Ethics Committee (EC)/Institutional Review Board (IRB) approved written informed consent

Exclusion criteria

* Pathological fracture * Additional acute fracture * Any not medically managed severe systemic disease * Recent history of substance abuse (i.e. recreational drugs, alcohol) that would preclude reliable assessment * Pregnancy or women planning to conceive within the registry period * Prisoner * Participation in any other medical device or medicinal product study within the previous month that could influence the results of the present registry

Design outcomes

Primary

MeasureTime frame
Number of complications within the first 3 months after surgery3 months

Secondary

MeasureTime frameDescription
Classification of the fracturePre-operatively (Day -1)Classification of the fracture using the Garden classification and the AO/AOTA classification
Time from injury to surgerySurgery (Day 0)Time in hours from the injury to the start of the surgery
Length of surgerySurgery (Day 0)Time in minutes from first incision to closure
Fracture mechanismPre-operatively (Day -1)Classification of the fracture mechanism in one of the following group: Fall from standing height , Falls from elevated height, Road traffic accident or Other causes
EQ5D-5LPre-operatively (Day -1), 6 weeks, 3 months, 6 months and 12 months after surgery
Radiological bone union (RUSH score)6 weeks, 3 months, 6 months and 12 months after surgeryRUSH score
Quality of reduction (Garden's alignment index and Lowell's criteria)Surgery (Day 0)Garden's alignment index and Lowell's criteria
Harris Hip ScorePre-operatively (Day -1), 6 weeks, 3 months, 6 months and 12 months after surgery

Countries

Austria, Germany, Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026