Actively Recruiting

Phase Not Applicable
Age: 60Years +
All Genders
NCT07244211

MAPT Protocol: Fixation Versus Arthroplasty Surgical Treatments for Early Recovery After HIP Fracture (FASTER-HIP)

Led by University of Southern California · Updated on 2026-05-13

600

Participants Needed

9

Research Sites

209 weeks

Total Duration

On this page

Sponsors

U

University of Southern California

Lead Sponsor

P

Patient-Centered Outcomes Research Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study is an intervention domain of the Musculoskeletal Adaptive Platform Trial. The primary goal of this pragmatic, randomized, open-label, comparative effectiveness trial is to evaluate if arthroplasty is superior to internal fixation when used to treat minimally displaced femoral neck fractures in older adults ≥60 years old. We hypothesize that arthroplasty will reduce death, preserve ambulation, increase days alive and out of hospital, and improve health status compared to internal fixation within 4 months and 12 months from randomization.

CONDITIONS

Official Title

MAPT Protocol: Fixation Versus Arthroplasty Surgical Treatments for Early Recovery After HIP Fracture (FASTER-HIP)

Who Can Participate

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 60 years of age or older undergoing surgery due to a minimally displaced femoral neck fracture
  • Health condition affecting physical mobility
  • Complete femoral neck fracture confirmed by hip X-rays, CT, or MRI
  • Fracture judged by surgeon to be treatable with either arthroplasty or internal fixation without reduction
  • Injury caused by low-energy mechanism
  • Availability of surgeons skilled in internal fixation and hip arthroplasty
Not Eligible

You will not qualify if you...

  • Patient not suitable for either treatment option
  • Expected survival less than 12 months
  • Terminal illness with survival under 12 months
  • Incarceration
  • Unable to provide informed consent due to language or lack of authorized representative
  • Problems maintaining follow-up
  • Enrollment in conflicting studies or prior enrollment in this trial domain
  • Declined participation or missed screening window
  • Other exclusions approved by data coordinating center
  • Associated lower limb injury preventing post-operative weight-bearing
  • Retained hardware around hip blocking study treatments
  • Infection around the hip
  • Pathologic fracture with a lytic lesion preventing internal fixation
  • Injury occurred more than 21 days before screening
  • Patient too ill for internal fixation or arthroplasty according to surgeon

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 9 locations

1

University of California, Irvine

Irvine, California, United States, 92660

Actively Recruiting

2

Los Angeles General Medical Center

Los Angeles, California, United States, 90033

Actively Recruiting

3

University of Southern California

Los Angeles, California, United States, 90033

Actively Recruiting

4

Indiana University

Bloomington, Indiana, United States, 47405

Actively Recruiting

5

University of Maryland, Baltimore - R Adams Cowley Shock Trauma Center

Baltimore, Maryland, United States, 21201

Actively Recruiting

6

University of Maryland Capital Region Health

Largo, Maryland, United States, 20774

Actively Recruiting

7

University of Mississippi

University, Mississippi, United States, 38677

Actively Recruiting

8

University of British Columbia

Vancouver, British Columbia, Canada, V6T 1Z4

Actively Recruiting

9

Fraser Health Authority

Vancouver, British Columbia, Canada

Actively Recruiting

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Research Team

J

Joseph Patterson, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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