Recovery of Patient Reported Outcomes After Intervention for Extremity Metastatic Bone Disease. (REPAIR)
Primary Objective
Determine whether patients undergoing prophylactic nail placement return to at least their preoperative pain interference (PI) and physical function (PF) scores by 6 weeks post operatively.
Description
If you join the study, you will still receive the standard of care for Metastatic Bone Disease (MBD) treatment/procedure as selected by your doctor. All data will be collected during the clinically necessary visits as per standard of care for your condition/procedure. If you give consent to enroll in the trial, we will be utilizing your completed surveys during your pre-operative visit and at the subsequent post-operative visits, 1 week, 2 week, 4 week, 6 week, 10 week, 3 month, 6 month, 1 year, and 2 year.
Details
Locations
University of Colorado Hospital
Principal Investigator
Steven Thorpe
Study ID
Protocol Number: 24-1586
More information available at ClinicalTrials.gov: NCT00000000
Categories
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