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Completed

NCT Number: NCT06338228

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

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.

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Grenoble Alpes University Hospital,La tronche

Grenoble, 38700, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. 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)

Secondary outcomes

  1. Define the prognostic factors associated with poor clinical outcomes and total hip replacement surgery

    Time frame: 1 year

    Prognostic factors from operative data

  2. Compare clinical and radiological findings with the literature

    Time frame: 1 year

    Clinical outcomes according to Harris Hip Score(HHS)

  3. Compare clinical and radiological findings with the literature

    Time frame: 1 year

    Clinical outcomes according to Oxford-12 HIP score (OXFORD HIP)

  4. Compare clinical and radiological findings with the literature

    Time frame: 1 year

    Clinical outcomes according to MAJEED SCORES

  5. 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

  6. Compare clinical and radiological findings with the literature

    Time frame: 1 year

    Clinical outcomes according to radiological scores

  7. 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)

  8. 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)

Sponsors and collaborators

Lead sponsor

University Hospital, Grenoble

Other

Registry information

Acronym: FANAD

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Mar 29, 2024
Registry last updated
Jan 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.