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Quality of Life and Function of Patients With Pelvic Tumors After Undergoing Hemipelvectomy

M.D. Anderson Cancer Center logo

M.D. Anderson Cancer Center

Status

Enrolling

Conditions

Malignant Primary Pelvic Neoplasm

Treatments

Other: Electronic Health Record Review
Other: Physical Performance Testing
Other: Questionnaire Administration
Other: Quality-of-Life Assessment

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT05134142
PA12-1046 (Other Identifier)
NCI-2021-11297 (Registry Identifier)

Details and patient eligibility

About

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.

Full 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.

Enrollment

200 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients within the institution who have undergone or will undergo a hemipelvectomy

Exclusion criteria

- None

Trial design

200 participants in 1 patient group

Observational (Physical tests, questionnaires, record review)
Description:
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.
Treatment:
Other: Quality-of-Life Assessment
Other: Questionnaire Administration
Other: Physical Performance Testing
Other: Electronic Health Record Review

Trial contacts and locations

1

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Central trial contact

Valerae O Lewis

Data sourced from clinicaltrials.gov

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