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

Quality of Life and Function of Patients After Hemipelvectomy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05134142
Enrollment
500
Registered
2021-11-24
Start date
2013-03-27
Completion date
2027-04-30
Last updated
2026-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malignant Primary Pelvic Neoplasm

Brief 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.

Detailed 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.

Interventions

OTHERElectronic Health Record Review

Undergo medical record review

OTHERPhysical Performance Testing

Undergo physical performance testing

OTHERQuality-of-Life Assessment

Complete assessments

OTHERQuestionnaire Administration

Complete questionnaire

Sponsors

M.D. Anderson Cancer Center
Lead SponsorOTHER
National Cancer Institute (NCI)
CollaboratorNIH

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

\- None

Design outcomes

Primary

MeasureTime frameDescription
Functions of patients who underwent internal hemipelvectomy with or without reconstruction or have had an external hemipelvectomyThrough study completion, average of 1 yearAll continuous variables including the scoring systems will be described as mean with standard deviation or median with range. Frequencies and percentages will be obtained for all categorical variables. Pediatric participants' data measures will be collected and analyzed separately from the adult populations.

Countries

United States

Contacts

CONTACTValerae O Lewis
volewis@mdanderson.org713-792-5073
PRINCIPAL_INVESTIGATORValerae O Lewis

M.D. Anderson Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 16, 2026