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Suspended Not applicable Interventional

Early Internal Fixation Versus NonOperative Care With Early Rehabilitation for LC1 Fragility Fractures of the Pelvis

ClinicalTrials.gov ID: NCT06496867

Public ClinicalTrials.gov record NCT06496867. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 1:14 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Multicenter Randomized Controlled Trial Comparing Early Internal Fixation Versus NonOperative Care With Early Rehabilitation for LC1 Fragility Fractures of the Pelvis: A Pilot Study

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The goal of this randomized pilot study is to assess feasibility of the trial and to collect information to inform the design of a definitive trial. Adult patients ages 60 years or older with a low-energy lateral compression type 1 (LC1) pelvis fracture with \<10 mm initial displacement of the posterior pelvic ring will be eligible to participate in the study. Patients will be randomized to one of two treatment groups, early internal fixation or nonoperative care with early rehabilitation, defined as at least five days of attempted mobilization by rehabilitation providers. Participants will be followed for 1 year.

Study identification

NCT ID
NCT06496867
Recruitment status
Suspended
Study type
Interventional
Phase
Not applicable
Enrollment
48 participants

Conditions and interventions

Eligibility (public fields only)

Age range
60 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 11, 2024
Primary completion
Dec 20, 2026
Completion
Dec 30, 2026
Last update posted
Aug 24, 2026

2024 – 2026

United States locations

U.S. sites
12
U.S. states
8
U.S. cities
10
Facility City State ZIP Site status
University of Arizona Phoenix Arizona 85006
Keck Medical Center of USC Los Angeles California 90033
Los Angeles General Medical Center Los Angeles California 90033
Cedars-Sinai Medical Center Los Angeles California 90048
University of California, Davis Sacramento California 95817
University of California San Francisco San Francisco California 94143
Indiana University Bloomington Indiana 47405
University of Maryland, Baltimore - R Adams Cowley Shock Trauma Center Baltimore Maryland 21201
Massachusetts General Hospital Boston Massachusetts 02114
The Curators of the University of Missouri - Missouri Orthopaedic Institute Columbia Missouri 65201
University of Utah Salt Lake City Utah 84112
University of Washington - Harborview Medical Center Seattle Washington 98104

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06496867, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 24, 2026 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06496867 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →