Restoring Mobility: Roles of Percutaneous Consolidation for Pelvic Ring Bone Lesions

Completed

• Conditions: Pelvic Ring Tumor Lesions

• Registration Number: NCT06155890
• Lead Sponsor: Centre Hospitalier Universitaire de Nice

Brief Summary

Evaluate early functional outcomes following percutaneous screw fixation or cementoplasty for pelvic ring tumor lesions.

Detailed Description

Not available

Study Timeline

• Study Start: 2016-01
• Primary Completion: 2023-09
• Study Completion: 2023-10
• Status Verified: 2023-11
• Study First Submitted: 2023-11-15
• Study First Submitted QC: 2023-11-24
• Study First Posted: 2023-12-05
• Last Update Submitted: 2024-11-28
• Last Update Posted: 2024-12-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 138

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
postoperative weight-bearing ambulation	During hospitalization, mainly less than 3 days	the ability of the patient to walk and bear weight after the procedure and its associated timeframe.

Secondary Outcome Measures

Name	Time	Method
Duration of hospitalization	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
Adverse event	During hospitalization, and follow-up	adverse event during procedure or hospitalization
Long-term effectiveness in preventing pathological fractures of the pelvic ring	3 months after the procedure, and during follow-up, up to 5 years	Absence of pelvic ring fracture during follow-up

Trial Locations

Locations (1)

CHU NICE; 🇫🇷 Nice, France