Antegrade Screw Placement Technique in Anterior Column of Acetabulum

Bakirkoy Dr. Sadi Konuk Training and Research Hospital

Status: Completed

Conditions: Acetabulum Fracture

Treatments: Other: No intervention

Study type: Observational

Funder types: Other

Identifiers

NCT06634251

2024/45-2024-04-01

Details and patient eligibility

About

This retrospective observational study aims to define the optimal antegrade entry point for screw placement in the anterior column fixation corridor (ACFC) of the acetabulum. Using fluoroscopic visualization techniques, the study examines computed tomography (CT) scans from 500 healthy adult patients to simulate screw placement and measure anatomical parameters. The goal is to determine patient-specific entry points and to assess the feasibility of screw placement using axial fluoroscopic views. The study also investigates gender-specific anatomical variations to provide insights for safer and more precise screw placement during anterior column fixation in pelvic surgery.

Full description

This study focuses on developing and validating a fluoroscopic visualization technique for identifying the optimal antegrade entry point (OAEP) in the anterior column fixation corridor (ACFC) of the acetabulum during pelvic surgery. Using three-dimensional reconstructions from pelvic computed tomography (CT) data of 500 healthy adults, the study simulates screw placement within the ACFC. A cylinder representing the screw is inserted virtually through the OAEP, ensuring that it remains within the confines of the fixation corridor without breaching its boundaries. The study records anatomical measurements, including the corridor's diameter, length, and the angles required for sagittal and coronal plane inclinations to visualize the OAEP.

The study also examines gender-specific anatomical variations, including differences in ACFC diameter, length, and required fluoroscopic angles. By defining patient-specific entry points and establishing a reliable fluoroscopic technique, this study aims to provide a practical and accessible method for anterior column fixation, minimizing complications and improving the safety and precision of screw placement in pelvic surgeries.

This novel approach has the potential to offer a cost-effective alternative to more expensive navigation systems, making it widely applicable in clinical settings.

Enrollment: 500 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients with pelvic computed tomography (CT) scans that provide complete anatomical details of the pelvis.
• Patients aged 18 to 65 years.
• Patients with fully matured bone structures, without evidence of fractures, deformities, or prior orthopedic surgery.
• Patients with no history of rheumatologic disease, advanced osteoporosis, bone metastasis, or metabolic bone disorders.

Exclusion criteria

• Patients with pelvic CT scans that do not fully display the anatomical structures.
• Patients younger than 18 years or older than 65 years.
• Patients with pelvic fractures, deformities, or prior orthopedic surgeries.
• Patients with incomplete clinical or radiological data.
• Patients with rheumatologic sequelae, bone metastasis, or metabolic bone diseases.

Trial design

500 participants in 2 patient groups

male group

Description:

This group consists of 250 healthy male adults whose pelvic CT scans were analyzed to define the optimal antegrade entry point and anatomical parameters for anterior column fixation. The fluoroscopic visualization technique and screw placement were simulated to assess anatomical variations and feasibility specific to the male cohort.

Treatment:

Other: No intervention

female group

Description:

This group consists of 250 healthy female adults whose pelvic CT scans were analyzed to define the optimal antegrade entry point and anatomical parameters for anterior column fixation. The fluoroscopic visualization technique and screw placement were simulated to assess anatomical variations and feasibility specific to the female cohort.

Treatment:

Other: No intervention