Outcomes after Sacroiliac Resection for Pelvic Malignancy

Overview

About this study

The purpose of this study is to gather clinical data to allow for comparisons in operative time, surgical technique, blood loss, level of resection, type of reconstruction, healing (based upon clinical report and imaging studies), transfusion requirements, complications, return to the operating room, and margins. There are other important data available that will also be recorded in order to draw comparisons to prior studies (Beadle, CORR 2005):  length of hospitalization, disposition at discharge, histology and grade of tumor, local recurrences, overall survival, duration of follow up, surgeon reported outcomes (MSTS 1987), chemotherapy regimen, radiation regimen, subsequent non-orthopedic oncologic surgeries.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Patients who underwent surgical intervention for a benign or malignant condition of the pelvis or sacrum where the sacroiliac joint was removed as part of the resection.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Matthew Houdek, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Additional contact information

Cancer-related trials contact form

Phone: 855-776-0015 (toll-free)

International patient clinical studies questions