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Clinical Trial Summary

This study aims to determine the functional outcomes of patients who underwent internal hemipelvectomy with or without reconstruction or external hemipelvectomy for pelvic tumors. Learning about the outcomes of these patients may help researchers determine the long-term effects of different types of hemipelvectomy procedures and may help improve quality of life.


Clinical Trial Description

PRIMARY OBJECTIVE: I. To determine functions of patients who underwent internal hemipelvectomy with or without reconstruction or have had an external hemipelvectomy. SECONDARY OBJECTIVES: I. To determine factors that influence the functional outcomes of these patients following surgery. II. Assess sexual and urinary function in patients who have undergone internal or external hemipelvectomy. III. Determine whether type of surgery influences long-term sexual and urinary function. OUTLINE: Patients undergo physical performance assessments and complete quality of life assessments and questionnaires pre-hemipelvectomy, at 6 weeks post-hemipelvectomy, and then every 3 months up to 12 months and yearly thereafter for 10 years. Patients who are 1 year out from surgery complete pain-related questionnaires once. Patients who have already undergone hemipelvectomy prior to enrollment undergo medical record review. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05134142
Study type Observational
Source M.D. Anderson Cancer Center
Contact Valerae O Lewis
Phone 713-792-5073
Email volewis@mdanderson.org
Status Recruiting
Phase
Start date March 27, 2013
Completion date April 30, 2025