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NCT07209280

Cannulated Bone Bolt® Screw System Versus Standard Cannulated Screw System Fixation for Pelvic Fractures

Sponsor: University of Utah

View on ClinicalTrials.gov

Summary

The investigators aim is to determine if the cannulated Bone Bolt® screw system will provide improved post-operative pain control as compared to standard cannulated screw system fixation for the operative treatment of LC1 fractures (primary outcome). Hypothesis: Patients treated with the cannulated Bone Bolt® screw system will experience a clinically important difference (1.5 points) in post-operative pain as measured by the Visual Analog Scale (VAS) compared to patients treated with standard cannulated screw system fixation.

Official title: Cannulated Bone Bolt® Screw System Versus Standard Cannulated Screw System Fixation for Lateral Compression Type-1 (LC-1) Pelvic Ring Injuries: Multicenter Prospective Observational Study

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

OBSERVATIONAL

Enrollment

100

Start Date

2025-06-11

Completion Date

2028-06

Last Updated

2025-10-06

Healthy Volunteers

No

Conditions

Interventions

OTHER

Cannulated Bone Bolt® Screw System

Patients treated with the Cannulated Bone Bolt® screw system for Lateral Compression Type -1 (LC-1) fractures.

OTHER

Standard Cannulated Screw System

Patients treated with the Standard Cannulated Screw System for Lateral Compression Type -1 (LC-1) fractures.

Locations (1)

University of Utah Orthopedics

Salt Lake City, Utah, United States