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Geriatric Lateral Compression 1 Pelvic Fractures

NCT05765669 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2025-06-13

No results posted yet for this study

Summary

Lateral compression-1 (LC1) pelvic ring fragility fractures cause significant pain and morbidity. These fragility injuries are associated with prolonged immobility and long hospital stays. Currently there is no consensus on operative stabilization of LC1 pelvic fractures, nor are there evidence-based guidelines to aid in management of these injury types. Furthermore, there is variability in operative indications, improvement in pain and mobilization. The purpose of this study is to compare percutaneous screw fixation to non-operative management in symptomatic LC1 fragility fractures in elderly patients.

Conditions

  • Lateral Compression 1 Pelvic Fracture

Interventions

PROCEDURE

Percutaneous screw fixation

Surgical intervention in the form of percutaneous screw fixation

OTHER

Pain management

Non-operative management in the form of pain management and physical therapy advanced with weightbearing as tolerated

OTHER

Physical therapy

Non-operative management in the form of pain management and physical therapy advanced with weightbearing as tolerated

Sponsors & Collaborators

  • Orthopaedic Trauma Association

    collaborator OTHER

  • Allina Health System

    collaborator OTHER

  • HealthPartners Institute

    lead OTHER

Principal Investigators

  • Mai P. Nguyen, MD · University of Minnesota and HealthPartners

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
60 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-05-05
Primary Completion
2026-06-01
Completion
2026-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05765669 on ClinicalTrials.gov