A New Decisional Tree for the Management of Acetabular Fractures : Monocentric Observational Study (FANAD)

January 6, 2026 updated by: University Hospital, Grenoble

Acetabular fractures are challenging fractures to treat. Many fracture patterns occur, in a deep anatomical area surrounded by numerous vascular and nervous elements, generally in a polytraumatic context . A reduction with less than 2 mm of incongruence is generally considered acceptable, limiting post-operative osteoarthritis that could rapidly require total hip arthroplasty. Due to the long learning curve, this surgery is limited to large reference centers

. In the last twenty years, the main series published in the literature are small series due to the rarity of the fractures and their trauma context (loss of follow-up, polytrauma patients…). The large variety of fracture patterns according to the Letournel classification creates a spread in patient distribution and decreases the power of statistical analysis. That is the reason why big series are rare and only a few of them allow significant conclusions . The other studies are meta-analyses with their limitations

The lack of consensus makes it difficult to interpret the results between series, so the investigators developed a decision tree to address this knowledge gap.

The aim of this study is to assess and compare the results of a decisional tree for acetabular fracture in a large cohort of patients from a well-known experimental trauma center.

Study Overview

Status

Completed

Study Type

Observational

Enrollment (Actual)

250

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Grenoble, France, 38700
        • Grenoble Alpes University Hospital,La tronche

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.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

All patients managed between 01/01/2020 and 01/01/2023 for an acetabular fracture in our trauma center are included in this single-center retrospective study.

The epidemiological data, the pre-operative management, the fracture patterns according to the Letournel and AO/OTA classification, the operative data and the radiological criteria (X-rays and CT scans) are retrospectively collected and analyzed.

Description

Inclusion Criteria:

  • Adult patient at the time of injury
  • Acetabular fracture
  • Pre-operative standard X-ray image
  • Pre-operative CT image
  • Post-operative X-ray standard image (AP-alar and obturator views)
  • Post-operative CT scan.
  • Willingness and ability to participate in the study

Exclusion Criteria:

  • Ipsilateral fracture femoral and/or associated pelvic ring fracture (Floating Hip C or B)
  • Pregnant, lactating women
  • Subject under administrative or judicial supervision

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
patients managed for Acetabular fracture
collect the data for all the patients managed and operated on between 01/01/2020 AND 31/01/2022 for Acetabular fracture

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The main objective of the study is to evaluate and compare the results of a decision tree for the management of acetabulum fractures (also called acetabulum) in a large cohort of patients from the trauma center at Grenoble University Hospital
Time Frame: 1 year
Clinical results according to the Postel-Merle d'Aubigné score (PMA)
1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Define the prognostic factors associated with poor clinical outcomes and total hip replacement surgery
Time Frame: 1 year
Prognostic factors from operative data
1 year
Compare clinical and radiological findings with the literature
Time Frame: 1 year
Clinical outcomes according to Harris Hip Score(HHS)
1 year
Compare clinical and radiological findings with the literature
Time Frame: 1 year
Clinical outcomes according to Oxford-12 HIP score (OXFORD HIP)
1 year
Compare clinical and radiological findings with the literature
Time Frame: 1 year
Clinical outcomes according to MAJEED SCORES
1 year
Compare clinical and radiological findings with the literature
Time Frame: 1 year
Clinical outcomes according to NUMERIC PAIN SCALE ( from 0-to10) 0 no pain 10 worst possible pain
1 year
Compare clinical and radiological findings with the literature
Time Frame: 1 year
Clinical outcomes according to radiological scores
1 year
Propose a new assessment of the traumatic hip joint based on PROMs (Patient Reported Outcomes Measures) via a dedicated digital application (Orthense by Digikare)
Time Frame: 1 year
Epidemiological data based on PROMs (Patient Reported Outcomes Measures) via a dedicated digital application (Orthense by Digikare)
1 year
Evaluation of Outcomes and Complications of Early Weight Bearing in Older Adults
Time Frame: 1 year
Complications intra-operative and postoperative (including complications of early weight bearing)
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Mehdi PI BOUDISSA, Pr, Grenoble Alpes University Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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 Major Dates

Study Start (Actual)

March 1, 2024

Primary Completion (Actual)

March 1, 2025

Study Completion (Actual)

March 1, 2025

Study Registration Dates

First Submitted

February 14, 2024

First Submitted That Met QC Criteria

March 26, 2024

First Posted (Actual)

March 29, 2024

Study Record Updates

Last Update Posted (Actual)

January 8, 2026

Last Update Submitted That Met QC Criteria

January 6, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2023-A02458-37

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Management of Acetabular Fractures

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