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Pediatric Hip Plate Versus Cannulated Screw in Pediatric Femoral Neck Fracture

An Multicenter Prospective Observational Study to Pediatric Hip Plate Versus Cannulated Screw in Pediatric Femoral Neck Fracture (Delbet Type II and III)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02803983
Acronym
PFNF
Enrollment
30
Registered
2016-06-17
Start date
2016-06-30
Completion date
2016-06-30
Last updated
2018-02-22

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

Conditions

Femoral Neck Fractures

Brief summary

The purpose of this study is to compare the early postoperative radiologic and clinical outcomes of pediatric hip plate and cannulated screw fixation in pediatric femoral neck fracture (Delbet type II and Delbet type III).

Detailed description

The children aged 3 to 14 years with femoral neck fracture that were treated with pediatric hip plate and cannulated screw fixation.

Interventions

PROCEDUREPediatric hip plate

Children were treated with pediatric hip plate.

PROCEDURECannulated screw

Children were treated with cannulated screw.

Sponsors

The Fuzhou No 2 Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
3 Years to 14 Years
Healthy volunteers
No

Inclusion criteria

* Patients with fractures that met these criteria, underwent definitive surgery and had complete clinical and radiographic follow up until fracture union at either institution were included in this study.

Exclusion criteria

* Pathologic fractures, and fractures in patients with osteogenesis imperfecta, neuromuscular disorders or any systemic disease that was associated with a predisposition to fractures or altered fracture healing were excluded.

Design outcomes

Primary

MeasureTime frameDescription
Radiographic unionThrough study completion, an average of 0.5 year.The time of radiographic union.

Secondary

MeasureTime frameDescription
The Ratliff classification standard scoreThrough study completion, an average of 1 year.Ratliff classification standard score was administered to determine the pain, function, activity and radiographic change.

Other

MeasureTime frameDescription
The complicationThrough study completion, an average of 1 year.The complication was evaluated by osteonecrosis, epiphyseal arrest, premature physeal closure, limb length discrepancy (over 3 cm) and internal fixation failure.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026