Clinical trial Recruiting at 1 site Observational Ages 80 and up

Evaluating cement treatment for pelvic bone lesions in elderly patients

Official title: Percutaneous Cementoplasty With or Without Screw Fixation for Bony Pelvis Lesions in Elderly Patients : Feasibility, Safety and Clinical Outcomes.

Run by Centre Hospitalier Universitaire de Saint Etienne · NCT05868863 · Data updated 2026-11-12

This study looks at whether a minimally invasive cement treatment can help older patients with pelvic bone fractures or tumors feel better and recover safely.

Quick facts

Study typeObservational
Ages80 Years and up
SexAll
Enrollment40 (estimated)
SponsorCentre Hospitalier Universitaire de Saint Etienne
Academic / other
Locations1 site (Saint-Etienne)
StatusRecruiting
StartedNovember 1, 2019
Main results expectedJune 2027
Study endsJune 2027
Registry record updatedSeptember 20, 2024
Trial IDNCT05868863 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are individuals aged 80 and over who have undergone percutaneous cementoplasty for pelvic bone lesions.

Probably not a fit

Patients who have received other interventional treatments at the same time and location may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to retrospectively assess the outcomes of percutaneous cementoplasty in patients aged 80 and over who have osteoporotic fractures or neoplastic lesions affecting the pelvis. The study will analyze data from medical records of patients treated at the university hospital center of Saint-Etienne between January 2012 and February 2023. The focus is on evaluating the feasibility, safety, and efficiency of this minimally invasive treatment approach, particularly for the elderly population who are often more fragile and at higher risk for such conditions.

Why it matters

Potential benefit: If successful, this treatment could significantly reduce pain and improve functional outcomes for elderly patients with pelvic bone lesions.

How similar studies have gone: While this approach is increasingly utilized, the specific outcomes of cementoplasty in this age group have not been extensively studied, making this a novel evaluation.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients with lesion of the bony pelvis treated by percutaneous cementoplasty with or without screw fixation at university hospital center of Saint-Etienne between January 1st 2012 and February 28th 2023

Exclusion Criteria:

* Other interventional treatment at the same time and at the same location

Where it's running

  • CHU Saint-Etienne
    Saint-Etienne, France
    Recruiting

Study contacts

  • Principal investigator: Sylvain GRANGE, MD — Centre Hospitalier Universitaire de Saint Etienne
  • Study coordinator: Sylvain GRANGE, MD
  • Email: grangesylvain@hotmail.fr
  • Phone: (0)477127827

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.