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Not yet recruitingNCT07871084Updated Oct 13, 2026

Functional Outcomes in Older Adults With Fragility Fractures of the Pelvis: The FFP-France Study

An observational study in Fragility Fractures of the Pelvis (FFP) and Osteoporotic Fractures, sponsored by Centre Hospitalier Universitaire de Nice. Not yet recruiting at 1 site in France. Open to participants aged 60 Years and older. Per ClinicalTrials.gov, last updated 2026-10-13.

Sponsored by Centre Hospitalier Universitaire de Nice · Observational

Updated Oct 13, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Other
Enrollment
200
Ages
60 Years and older
Sex
All
01

Study summary

Fragility fractures of the pelvis (FFP) are an increasingly common complication of osteoporosis in older adults and are associated with substantial morbidity, loss of independence, and mortality. Despite their clinical impact, FFP remain underdiagnosed, particularly sacral fractures, and their management varies considerably across centers.FFP-France is a French multicenter ambispective observational study designed to describe functional outcomes in adults aged 60 years and older with FFP. The primary objective is to assess functional outcome at 6 months using the Parker Mobility Score. Secondary objectives include describing clinical and radiological characteristics, diagnostic and therapeutic management, pain, autonomy, mortality, osteoporosis management, and factors associated with unfavorable functional recovery.

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Conditions studied

  • Fragility Fractures of the Pelvis (FFP)
  • Osteoporotic Fractures

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03

In context

Osteoporotic Fractures

94 studies on the registry are indexed under Osteoporotic Fractures; 23 are open to participants now.

This study's planned enrollment of 200 is below the median of 255 across 39 observational studies indexed under Osteoporotic Fractures.

Browse Osteoporotic Fractures studies →

Lead sponsor

Centre Hospitalier Universitaire de Nice is the lead sponsor of 722 studies on the registry; 176 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
60 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adults aged 60 years and older diagnosed with a fragility fracture of the pelvis and managed at participating French centers during the retrospective or prospective study periods.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age ≥60 years.
  • Fragility fracture of the pelvis occurring spontaneously or following a low energy trauma.
  • Fracture confirmed by imaging (radiography, computed tomography, magnetic resonance imaging, bone scintigraphy, or positron emission tomography).

Exclusion criteria

Exclusion Criteria:

  • Pelvic fracture resulting from high-energy trauma.
  • Pathological fracture secondary to a malignant bone lesion.
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Study design

Observational model
Cohort
Time perspective
Other
Enrollment
200 participants (estimated)
Patient registry
No

Groups and cohorts

  • Patients With Fragility Fractures of the Pelvis

    Other: Observational Assessment of Fragility Fractures of the Pelvis

Interventions

  • OtherObservational Assessment of Fragility Fractures of the Pelvis

    No study-specific intervention is performed. Diagnostic and therapeutic management is determined by routine clinical practice at each participating center. Clinical, radiological, treatment, and outcome data are collected for observational purposes.

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What researchers measure

Primary outcomes

  1. Functional Mobility at 6 Months Assessed by the Parker Mobility Score (PMS)

    Functional mobility will be assessed using the Parker Mobility Score (PMS), which evaluates the participant's ability to walk indoors, walk outdoors, and go shopping. Each item is scored from 0 to 3, resulting in a total score ranging from 0 to 9, with higher scores indicating greater mobility.

    Time frame: 6 months after the fragility fracture of the pelvis

Secondary outcomes

  1. Type of Fracture Management

    Proportion of patients managed conservatively or interventionally for fragility fracture of the pelvis. Management strategies will be described according to patient characteristics and fracture type, including the Rommens classification

    Time frame: From diagnosis to 12 months after the fracture

  2. Use of Anti-Osteoporotic Treatment

    Proportion of patients receiving anti-osteoporotic treatment after the fracture. Anti-osteoporotic treatment before and after the fracture, including treatment initiation, continuation, or modification during follow-up, will be recorded.

    Time frame: From diagnosis to 12 months after the fracture

  3. Recovery of Pre-Fracture Mobility

    Proportion of patients who recover their pre-fracture level of mobility at 3 and 12 months, based on the Parker Mobility Score. The Parker Mobility Score ranges from 0 to 9, with higher scores indicating better mobility. Demographic and clinical characteristics, fracture type, fracture management strategy, and osteoporosis management will be investigated as potential factors associated with functional recovery.

    Time frame: 3 and 12 months after the fracture

  4. All-Cause Mortality

    Proportion of patients who die from any cause during follow-up. Mortality will be assessed at 3, 6, and 12 months after the fracture

    Time frame: 3, 6, and 12 months after the fracture

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Study locations

1 site
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Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 13, 2026
Show all 1 update
  1. Oct 13, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07871084
Responsible party
Sponsor
First posted
Oct 13, 2026
Start date
Dec 1, 2026 (estimated)
Primary completion
May 31, 2029 (estimated)
Completion
Nov 30, 2029 (estimated)
Last update
Oct 13, 2026

Study contacts

Marie-Charlotte TROJANI
Contact
marie-charlotte.trojani@univ-cotedazur.fr
0492549777 ext. +33

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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