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Clinical Trials/NCT06293495
NCT06293495
Not yet recruiting
Not Applicable

Comparison of the Incidence of Cut-out Between Intramedullary Nails With Double Cephalic Screw vs. Unique in Pertrochanteric Fractures: a Prospective Randomized Clinical Trial

Puerta de Hierro University Hospital1 site in 1 country200 target enrollmentMarch 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Proximal Femoral Fractures
Sponsor
Puerta de Hierro University Hospital
Enrollment
200
Locations
1
Primary Endpoint
Incidence of cut-out.
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

The goal of this clinical trial is to compare outcomes in the treatment of proximal femur fractures. The main question it aims to answer is whether the use of a double cephalic screw prevents nail failure (cut-out).

Participants will be treated using open reduction and internal fixation with a proximal femoral nail. Researchers will compare intramedullary nailing with a single cephalic screw (Gamma nail) and with a double cephalic screw (Chimaera nail) to see the cut-out rate.

Detailed Description

Randomized, open and prospective clinical trial. Following the surgical indication for open reduction and internal fixation as treatment for proximal femoral fractures, patients will be randomly assigned (ratio 1:1) to one of the following treatments: Control group: a Gamma 3 nail (single cephalic screw system) will be used for osteosynthesis of the fracture. Experimental group: a Chimaera nail (system with double cephalic screw) will be used for osteosynthesis of the fracture. Patient (or their legal guardian) must provide/sign the informed consent prior to inclusion in the study. After the surgery, patients will be followed-up at 6 weeks, 3 and 6 months. At those times, data related to the radiological examination, the appearance of complications and the walking ability evaluation scale (FAC) will be collected.

Registry
clinicaltrials.gov
Start Date
March 1, 2024
End Date
April 1, 2026
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Puerta de Hierro University Hospital
Responsible Party
Principal Investigator
Principal Investigator

Pedro-José Torrijos-Garrido

Principal Investigator

Puerta de Hierro University Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients with proximal femur fracture (OTA/AO 31-A1, A2 and A3) requiring surgical treatment.
  • Signing of written informed consent according to current legislation before collecting any information, either by the patient or by the legal representative or by people linked by family ties.

Exclusion Criteria

  • Presence of other fractures in the ipsilateral femur that condition the surgical treatment of the pertrochanteric femur fracture.
  • Subcapital fracture of the proximal femur.
  • Subtrochanteric fracture of the proximal femur.
  • Pathological fracture.

Outcomes

Primary Outcomes

Incidence of cut-out.

Time Frame: 0-6 months

Cut-out is a mechanical complication consisting of varus collapse and migration of the cephalic screw through the femoral head.

Secondary Outcomes

  • Number of Surgical complications (post-operative)(0-6 months)
  • Baumgaertner reduction quality criteria(3-6 months)
  • Number of Surgical complications (Intraoperative)(0-1 month)
  • Functional Ambulatory Categories (FAC)(0-6 months)
  • Tip-apex distance(3-6 months)
  • Parker index(3-6 months)

Study Sites (1)

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