Back to search results
NCT07209280

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

Enrolling by Invitation
Not specifiedAges 18–80Observational
University of Utah
~100 participants
Updated 2026-04-23 on ClinicalTrials.gov
What's tested:Cannulated Bone Bolt® Screw SystemStandard Cannulated Screw System

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Visual Analog Scale (VAS) pain
Measured over 2-weeks after surgery
+2 more outcomes measured

Conditions

Pain

Explore related trials

Lateral Compression Type-1 Pelvic Ring Fracture

Where it's being run

1 sites across 1 states
Utah1

Study leadership

  • Lucas Marchand, M.D. · PRINCIPAL_INVESTIGATOR · University of Utah Orthopaedics

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

Age at presentation between 18 and 80 years in line with literature from prior investigations.
Operative LC1 pelvic ring injury.
Glasgow Coma Scale of 15.
Willingness to participate in study.

Exclusion

Inability to provide informed consent.
Pregnant or lactating woman.
Current incarceration.
Associated spinal cord injury.
Non-ambulatory patients (including patients with associated lower extremity fracture that may limit post-operative weight bearing).
Patient presents with osteoporosis, which in the opinion of the Principal Investigator, may limit the subject's ability to support fracture repair using the study device.
Patient has a metabolic disorder that may impair bone formation.
Patient has osteomalacia.
Patient has distant foci of infections which may spread to the implant site or patient with infection, sepsis or osteomyelitis.
Patient has a vascular insufficiency, muscular atrophy, or neuromuscular disease.
Patient is a current alcohol or drug abuser.
Patients unable to comply with post-operative instruction.
Other lower extremity injuries that impact weight bearing recommendation.
Injuries that may have a larger impact on pain than the studied pelvic ring.
Non-English/Spanish speaking.

What this trial measures

  • Visual Analog Scale (VAS) pain2-weeks after surgery

    VAS pain score (0 no pain - 10 severe pain)

  • Visual Analog Scale (VAS) pain6-weeks after surgery

    VAS pain score (0 no pain - 10 severe pain)

  • Visual Analog Scale (VAS) pain12-weeks after surgery

    VAS pain score (0 no pain - 10 severe pain)