RECRUITING

Rim Plate to Buttress Plate for Posterior Wall Acetabular Fractures With and Without Inter-fragmentary Screws

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Conditions

Acetabular Fracture

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The hypothesis of this study is that the Rim Plate method utilizing interfragmentary screws placed through the plate will result in superior fixation, a lower rate of loss of reduction of the fracture fragment, better anatomic healing of the articular (joint) surface, a decreased rate of early post-traumatic arthritic changes of the joint (cartilage) surface, and improved functional outcomes.

Official Title

A Randomized Prospective Study Comparing Rim Plate to Buttress Plate for Posterior Wall Acetabular Fractures With and Without Inter-fragmentary Screws

Quick Facts

Study Start:2023-08-01
Study Completion:2026-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06409559

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Skeletally mature males and females, ≥ 18 years old and with age less than 65 years.
  2. 2. Fracture of the acetabular posterior wall fracture due to acute traumatic hip dislocation, confirmed with anteroposterior pelvic or hip radiographs, and CT scan
  3. 3. Operative fixation of fractures within 14 days of presenting to the emergency room.
  4. 4. Patient was ambulatory prior to fracture, with or without walking aids
  5. 5. Medically optimized for operative intervention
  6. 6. Provision of informed consent by patient or legal guardian.
  1. 1. Patients not suitable for internal fixation (severe osteoarthritis, rheumatoid arthritis, or pathologic fracture).
  2. 2. Pre-existing orthopedic fixation, implant, or prosthesis around the affected acetabulum.
  3. 3. Patients with metabolic bone disease including diagnosis of osteoporosis.
  4. 4. Patients with bony or soft tissue infections around the acetabulum.
  5. 5. Patients unable to provide informed consent.
  6. 6. Patients having other fractures of Pelvis or acetabulum other than an isolated posterior acetabular wall fracture.
  7. 7. Patients with previous history of acetabular fracture (operative or nonoperative)
  8. 8. Patients with previous history of hip pathology such as avascular necrosis, hip dysplasia, Legg-Calve Perthes Disease, or advanced degenerative arthritis.

Contacts and Locations

Study Contact

Kimberly A Hasselfeld
CONTACT
5135581933
hasselky@uc.edu

Study Locations (Sites)

University of Cincinnati College of Medicine
Cincinnati, Ohio, 45267
United States

Collaborators and Investigators

Sponsor: University of Cincinnati

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-08-01
Study Completion Date2026-03

Study Record Updates

Study Start Date2023-08-01
Study Completion Date2026-03

Terms related to this study

Additional Relevant MeSH Terms

  • Acetabular Fracture