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Femoral Neck FracturesFNSNCT04577261

FNS (FEMORAL NECK SYSTEM) Study

An observational study of Femoral Neck Fractures, run by Wake Forest University Health Sciences at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

A post-market, prospective study to evaluate the reoperation rate of displaced and nondisplaced femoral neck fractures treated with the Femoral Neck System (FNS)™ Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Femoral Neck Fractures
How many people
43 participants
Where
1 siteUnited States
Study dates
7 Oct 2020to 2 Apr 2026
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Subject has experienced displaced or non-displaced intracapsular femoral neck fracture

Who may be able to join

  • The subject must provide written informed consent
  • The subject must be eighteen (18) years of age or older.
  • The subject must be willing and able to make all required study visits including one (1) year post-operative follow-up.
  • The subject must be able to follow instructions.
  • Subject has experienced displaced or non-displaced intracapsular femoral neck fracture

Who cannot join

  • Subject with fracture occurring more than 7 days prior to the date of surgery
  • Subject has more than one fracture on target extremity.
  • Subject is obese as defined by a Body Mass Index (BMI) > 45 at the time of surgery.
  • Subject, in the opinion of the Investigator, has an emotional or neurological condition that preludes cooperation and compliance with the rehabilitation regimen.
  • Therapy with another investigational agent within thirty (30) days of Screening or planned therapy with another investigational agent during the course of the study.
  • Subject has a physical condition that, in the opinion of the Investigator, would preclude adequate implant support or impede healing (e.g. blood supply impairment insufficient bone quality or quantity, or an active, local or systemic infection). If this is identified at the time of surgery, the subject will be screen failed.
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  • Subject has undergone previous surgery on the target hip.
  • Current systemic therapy with cytotoxic drugs.
  • Subjects with a history of poor compliance with medical treatment.
  • Subjects with a medical or physical condition that, in the opinion of the Investigator, would preclude safe subject participation in the study.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Wake Forest Health Sciences

    Winston-Salem, North Carolina, 27157

Other trials in United States

About this study

Official title: A Prospective Study To Evaluate The FEMORAL NECK SYSTEM (FNS) In The Treatment Of INTRA-CAPSULAR FEMORAL Neck Fractures

A post-market, prospective study to evaluate the reoperation rate of displaced and nondisplaced femoral neck fractures treated with the Femoral Neck System (FNS)™

Read the detailed description

To evaluate the re-operation rate for any reason of displaced and non-displaced femoral neck fractures treated with the Femoral Neck System (FNS)™ at one year post-operation. The Femoral Neck System (FNS)™ represents a new generation of implants designed to improve outcomes in the treatment of femoral neck fractures. These implants offer a fixed angle construct and all of its mechanical advantages with regards to neutralizing shear and providing stability while not exerting a rotational malreduction force on the fracture. The FNS system has been shown to compare favorably to traditional fixed angle constructs in a cadaveric model

Keywords
neck fractures, implant failure, osteotomy
Medical subject headings
Femoral Neck Fractures

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT04577261
Study groupRoleWhat they receive
Femoral Neck System (FNS) ParticipantsParticipants who will undergo surgery to treat a fractured femoral neck using the FNS (Femoral Neck System)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Re-operation rate

    Re-operation rate for any reason of displaced and non-displaced femoral neck fractures treated with the Femoral Neck System (FNS)™

    Measured: Year 1 post-operation

Secondary outcomes (13)
  1. Timed Up and Go (TUG) time

    The Timed Up and Go Test assesses mobility, balance, walking ability, and fall risk in adults by measuring time, in seconds, that it takes the individual to stand from a chair, walk a distance of 10 feet, walk back to the chair, and sit down. The subject will perform the test in their everyday footwear with their walking aid (cane, walker), if applicable. Normal healthy elderly usually complete the task in ten seconds or less. Very frail or weak elderly with poor mobility may take 2 minutes or more. 8

    Measured: Week 6, Months 3, 6, and 12

  2. European Quality of Life 5 Dimensions 5 Level Version (EQ-5D-5L) Score

    The EuroQol EQ-5D-5L is a standardized instrument for use as a measurement of health outcome. It consists of a descriptive system with 5 dimensions (mobility, self-care, usual activities, pain/discomfort and anxiety/depression), which are each assigned five levels (no problems, slight problems, moderate problems, severe problems and extreme problems) The first part (descriptive system with 5 dimensions) is scored using the Health state index scores. Health state index scores generally range from less than 0 (where 0 is the value of a health state equivalent to dead; negative values representing values as worse than dead) to 1 (the value of full health), with higher scores indicating higher health utility.

    Measured: Baseline, Week 6, Months 3, 6, and 12

  3. European Quality of Life 5 Dimensions 5 Level Version (EQ-5D-5L) - VAS (Visual Analogue Scale) Score

    The EuroQol EQ-5D-5L is a standardized instrument for use as a measurement of health outcome. It consists of a descriptive system with 5 dimensions (mobility, self-care, usual activities, pain/discomfort and anxiety/depression), which are each assigned five levels (no problems, slight problems, moderate problems, severe problems and extreme problems), as well as, a Visual Analogue Scale where subjects indicate a numerical value from 0-100 where 0 is the worst imaginable health state and 100 is the best imaginable health state.

    Measured: Baseline, Week 6, Months 3, 6, and 12

  4. Visual Analogue Scale (VAS) for Pain Score

    The Visual Analogue Scale is simply a line of fixed length, on which the subject marks their experience of pain with a single stroke of a pen - The subject will record their level of pain on a 100 mm visual analog scale - the scale will be marked 'no pain' on the left side of the scale and 'severe pain' at the right end of the scale - It is generally accepted that a pain VAS score of 30, 70, and 100 indicates the upper boundaries of mild, moderate, and severe pain intensity

    Measured: Baseline, Week 6, Months 3, 6, and 12

  5. Number of Participants with Quality of Fracture Reduction

    Appropriate reduction will be defined as the principal compressive trabeculae measuring >160° in the AP view and <5° of posterior angulation in the lateral view. If reduction is acceptable in both views, it will be classified as grade I. Grade II will be indicative of one plane of malreduction, and grade III will be indicative of malreduction in both radiographic views.

    Pre-operative radiographs will be reviewed and classified as displaced (e.g. Garden III \& IV) or non-displaced (e.g. Garden I \& II) femoral neck fractures by the Investigator at each site Pauwel Classification (Type I - 30 degrees, Type II - 50 degrees, Type III - 70 degrees)

    Measured: Baseline, Week 6, Months 3, 6, and 12

  6. Active Straight Leg Raise (ASLR) Assessment Score

    The ALSR assessment provides information about the ability of load transfer and motor control strategies in the lumbo/pelvic/hip complex. ASLR will be performed with the subject in a relaxed supine position with legs straight and feet apart. Subjects will be instructed to raise their operated leg 20cm above the examination table without bending the knee and without pelvic movement relative to the trunk. A score will be provided by the subject for the operated limb on a six-point Likert scale (0 = not difficult at all, 1 = minimally difficult; 2 = somewhat able to do, 3 = fairly difficult, 4 = very difficult, 5 = unable to do) -Lower score denotes better outcome

    Measured: Baseline, Week 6, Months 3, 6, and 12

  7. Number of Participants with Intraoperative complications

    Number of Participants with Intraoperative complications

    Measured: Baseline, Week 6, Months 3, 6, and 12

  8. Radiographic outcomes including quality of fracture reduction

    Perform radiology imaging collecting both anteroposterior (AP) and lateral images of the target hip to ensure the FNS is properly implanted - (healed, non-union, aligned, mal-union, osteonecrosis of femoral head, no osteonecrosis of femoral head, none)

    Measured: Baseline, Week 6, Months 3, 6, and 12

  9. Number of Construct failure past 6 months

    Construct failure past typical femoral neck fracture healing period (past 6 months)

    Measured: Months 6 and 12

  10. Time to return to full weight-bearing

    Time to return to full weight-bearing

    Measured: Week 6, Months 3, 6, and 12

  11. Ambulatory status from pre-injury to study completion

    Subjects will be assessed as "Unaided", "Using a cane", "Using a walker" or "Bed to Chair"

    Measured: Baseline, Week 6, Months 3, 6, and 12

  12. Length of hospital stay

    Length of hospital stay

    Measured: Week 6, Months 3, 6, and 12

  13. Number of Hospital readmission for any reason

    Number of Hospital readmission for any reason

    Measured: Week 6, Months 3, 6, and 12

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Oct 2020
  2. Study start7 Oct 2020
  3. Primary completion2 Apr 2026
  4. Study completion2 Apr 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
43 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04577261
Sponsor's protocol ID
IRB00066583
Acronym
FNS
Status last verified
Apr 2026
First submitted
30 Sep 2020
Last updated
4 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Kenan S, Gold A, Salai M, Steinberg E, Ankory R, Chechik O. Long-Term Outcomes Following Reduction and Fixation of Displaced Subcapital Hip Fractures in the Young Elderly. Isr Med Assoc J. 2015 Jun;17(6):341-5.

    PubMed 26233991
  • Han S, Oh M, Yoon S, Kim J, Kim JW, Chang JS, Ryu JS. Risk Stratification for Avascular Necrosis of the Femoral Head After Internal Fixation of Femoral Neck Fractures by Post-Operative Bone SPECT/CT. Nucl Med Mol Imaging. 2017 Mar;51(1):49-57. doi: 10.1007/s13139-016-0443-8. Epub 2016 Aug 11.

    PubMed 28250858
  • Farooq MA, Orkazai SH, Okusanya O, Devitt AT. Intracapsular fractures of the femoral neck in younger patients. Ir J Med Sci. 2005 Oct-Dec;174(4):42-5. doi: 10.1007/BF03168981.

    PubMed 16445160
  • Campenfeldt P, Hedstrom M, Ekstrom W, Al-Ani AN. Good functional outcome but not regained health related quality of life in the majority of 20-69 years old patients with femoral neck fracture treated with internal fixation: A prospective 2-year follow-up study of 182 patients. Injury. 2017 Dec;48(12):2744-2753. doi: 10.1016/j.injury.2017.10.028. Epub 2017 Oct 18.

    PubMed 29106948

Questions about this trial

What is this clinical trial studying?

An observational study of Femoral Neck Fractures, run by Wake Forest University Health Sciences at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 4 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Re-operation rate (time frame: Year 1 post-operation). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04577261, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 May 2026.

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