CHU NICE
Nice, France
NCT Number: NCT06155890
Evaluate early functional outcomes following percutaneous screw fixation or cementoplasty for pelvic ring tumor lesions.
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Nice, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion :
Exclusion criteria
Time frame: During hospitalization, mainly less than 3 days
the ability of the patient to walk and bear weight after the procedure and its associated timeframe.
Time frame: During hospitalization, and follow-up
adverse event during procedure or hospitalization
Time frame: Mainly less than 3 days
The duration of hospitalization will be measured between the day and time of arrival at the hospital and the day and time of discharge from the hospital
Time frame: 3 months after the procedure, and during follow-up, up to 5 years
Absence of pelvic ring fracture during follow-up
Centre Hospitalier Universitaire de Nice
Other
Restoring Mobility: Roles of Percutaneous Consolidation for Pelvic Ring Bone Lesions -a Multicenter Study
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.