Quality of Life and Function of Patients With Pelvic Tumors After Undergoing Hemipelvectomy
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- STATUS
- Recruiting
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- participants needed
- 200
-
- sponsor
- M.D. Anderson Cancer Center
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.
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.
OUTLINEPatients 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.
Details
| Condition | Malignant Primary Pelvic Neoplasm |
|---|---|
| Treatment | Questionnaire Administration, Quality-of-Life Assessment, Electronic Health Record Review, Physical Performance Testing |
| Clinical Study Identifier | NCT05134142 |
| Sponsor | M.D. Anderson Cancer Center |
| Last Modified on | 26 November 2021 |
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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