MedPath

CM Asia Nail With AS2 Without AS2 (AS2 Study)

Not Applicable
Completed
Conditions
Trochanteric Fracture of Femur
Interventions
Procedure: Open Reduction and Internal Fixation
Device: ZNN CM Asia
Device: Anterior Support Screw
Registration Number
NCT03196193
Lead Sponsor
Zimmer Biomet
Brief Summary

The purpose of this study is to compare reduction positon maintenance rate at 3 weeks post-operatively between patients operated with Anterior Support Screw (AS2) and without AS2 technique in RCT setting. Total 240 cases(each arm 120 cases) will be enrolled at maximum 15sites, total study duration is 22months.

Detailed Description

Objective: To compare fracture reduction maintenance rate at 2-3weeks post-operatively between patients operated with AS2 (investigational group) and patients operated without AS2 (Control group) using same implant system (ZNN CM Asia, Zimmer Biomet).

Endpoint: Primary: The rate of reduction position maintenance at 2-3 weeks post-operatively. Secondary: Surgery time / fracture type / postoperative reduction position / CT assessment / Safety information

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
240
Inclusion Criteria

In order to be eligible to participate in this study, a subject must meet all of the following criteria.

  • Eligible for intramedullary nailing.
  • Fracture type is classified as 3-partB or 4-part fracture in 3D-CT (Three Dimensional Computed Tomography) classification (Nakano), and combination with a subtype P in lateral classification (Ikuta) at preoperative CT (Computed Tomography) assessment.(In the case of classified in radiograph (X-ray) at preoperative: Classified as Type 4 or Type 5 in Jensen classification, and combination of subtype P in lateral classification (Ikuta))
  • Japanese Male or female
  • > 20 years of age
  • Primary closed intertrochanteric fracture of the femur
  • Subjects willing to return for follow-up evaluations.
Exclusion Criteria

A potential subject who meets any of the following criteria will be excluded from participation in this study.

  • Patient who cannot take CT image within 3 days and 2-3weeks after surgery.
  • Uncooperative patient or patient with neurologic disorders who are incapable of following directions.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
ZNN CM Asia without AS2 techniqueZNN CM AsiaTrochanteric Fracture treated by Open Reduction and Internal Fixation using with ZNN CM Asia nail without additional screw fixation.
ZNN CM Asia with AS2 techniqueOpen Reduction and Internal FixationOpen Reduction and Internal Fixation with AS2 Trochanteric Fracture treated by Open Reduction and Internal Fixation using with ZNN CM Asia nail. Bone fragment will be stabilized by additional screw fixation (Anterior Support Screw).
ZNN CM Asia with AS2 techniqueZNN CM AsiaOpen Reduction and Internal Fixation with AS2 Trochanteric Fracture treated by Open Reduction and Internal Fixation using with ZNN CM Asia nail. Bone fragment will be stabilized by additional screw fixation (Anterior Support Screw).
ZNN CM Asia with AS2 techniqueAnterior Support ScrewOpen Reduction and Internal Fixation with AS2 Trochanteric Fracture treated by Open Reduction and Internal Fixation using with ZNN CM Asia nail. Bone fragment will be stabilized by additional screw fixation (Anterior Support Screw).
ZNN CM Asia without AS2 techniqueOpen Reduction and Internal FixationTrochanteric Fracture treated by Open Reduction and Internal Fixation using with ZNN CM Asia nail without additional screw fixation.
Primary Outcome Measures
NameTimeMethod
Number of Patient With and Without Excessive Lag Screw Sliding DistancePostoperative 2-3 week

Number of patient was counted based on CT measurement results. Relative position of lag screw between CT images taken at both immediate and 2-3 weeks postoperatively was measured and recorded in value (e.g., 1.5 mm). This was called as "lag screw sliding distance". Four millimeter was set as threshold to define success and failure. Less than 4mm of lag screw sliding distance was recognized as Success and equal to or more than 4mm of lag screw sliding distance was recognized as Failure.

Secondary Outcome Measures
NameTimeMethod
Intraoperative SafetyIntraoperative

This is to evaluate whether any adverse events specific to insert additional screw for AS2 technique were occurred.

Surgery TimeIntraoperative, an average of 1 hour

Surgery time from skin incision to closure

Image Assessment Using Computed Tomography (CT)2-3 weeks postoperatively

Number of patient was counted based on CT measurement results. When the fracture reduction position achieved at surgery was maintained at 2 to 3 weeks, then the patient was categorized as success (Reduction position maintained). On the other hand, patient was categorized as failure (Reduction position changed) in the case that the fracture reduction position was changed.

Fracture repair position was categorized into three; "Anterior", "Neutral" or "Posterior" based on relative position of proximal bone fragment and distal bone fragment.

This analysis only includes patients whose fracture reduction position at immediate postoperative CT was either "Anterior" or "Neutral".

If both immediate and 2-3 weeks postoperative CT images show same fracture reduction position (example: "Anterior" at immediate postoperatively \& "Anterior" at 2-3 weeks postoperatively), then the patient was recognized as Success (Reduction position maintained).

Trial Locations

Locations (12)

Kure Kyosai Hospital

🇯🇵

Kure, Hiroshima, Japan

Toyooka Hospital

🇯🇵

Toyooka, Hyogo, Japan

Kasugai Municipal Hospital

🇯🇵

Aichi, Kasugai, Japan

Hoshigaoka Medical Center

🇯🇵

Hirakata, Osaka, Japan

Numazu City Hospital

🇯🇵

Numazu, Shizuoka, Japan

Okayama Red Cross Hospital

🇯🇵

Okayama, Japan

Saiseikai Kumamoto Hospital

🇯🇵

Kumamoto, Japan

Saiseikai Takaoka Hospital

🇯🇵

Takaoka, Toyama, Japan

Kyushu Central Hospital

🇯🇵

Fukuoka, Japan

Niigata Central Hospital

🇯🇵

Niigata, Japan

Okayama Rosai Hospital

🇯🇵

Okayama, Japan

Saga Pref. Medical Centre Koseikan

🇯🇵

Saga, Japan

© Copyright 2025. All Rights Reserved by MedPath