Percutaneous Cementoplasty With or Without Screw Fixation
ConditionInterventional Radiology
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age80+
SponsorCentre Hospitalier Universitaire de Saint Etienne
About this trial
Bone pathologies such as fragility fractures and neoplastic bone lesions are frequently encountered in rheumatology. When these lesions affect the pelvis, they are responsible both for pain that is sometimes very disabling, but also for significant functional disorders due to their location.
Different methods may be used to treat these lesions. The current challenge is to use less and less invasive techniques such as radio-guided cementoplasty to be able to treat all types of people, especially the most fragile. Among the elderly, the prevalence of these bone pathologies continues to increase due to the aging of the population and the improvement of diagnostic means.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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
Disqualifiers
Other interventional treatment at the same time and at the same location
Trial population
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 will be included.
Trial design
Design model
Cohort
Time perspective
Retrospective
Treatments tested in this trial
datas of medical record.
Other interventionAnalysis datas of medical record: * Feasibility of the technique * Safety of the technique with evaluation by Cardiovascular and Interventional Radiological Society of Europe (CIRSE) scale * Analgesic intake before and after the procedure * Functional criteria: early rising, walking
Treatment groups
40 Participants
are divided into 1 treatment groupGroup A: osteoporotic fractures or neoplastic lesions of the bony pelvis1 intervention
Trial outcomes
Primary outcomes
1
Feasibility of the technique
Collect from medical records the number of procedures that were completed and performed as theoretically intended.
Time frame
Months: 3Secondary outcomes
1
Safety of the technique by number of adverse events
collected in the medical record
Time frame
Months: 32
Number of Analgesic intake before and after the procedure
collected in the medical record
Time frame
Months: 33
Analysis Functional criteria: walking
Collect from medical record the number of patients who can walk before and after the procedure.
Time frame
Months: 34
Analysis Functional criteria: early rising
Collect from medical record the number of patients who can rise before and after the procedure.
Time frame
Months: 3Sponsors and contacts
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Source ClinicalTrials.gov