Recruiting

Observational Study

Sponsor:

M.D. Anderson Cancer Center

Code:

NCT05134142

Conditions

Malignant Primary Pelvic Neoplasm

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Not accepted

Interventions

Electronic Health Record Review

Physical Performance Testing

Quality-of-Life Assessment

Questionnaire Administration

Study Details

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.

Conditions

Malignant Primary Pelvic Neoplasm

Study ID

NCT05134142

Start date

Mar 27, 2013

Status verified date

May, 2026

Completion date

Apr 30, 2027

Anticipated

Primary completion date

Apr 30, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Not accepted

Inclusion Criteria:

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

Exclusion Criteria:

\- None

Study Design

Enrollment

200 participants

Anticipated

Interventions and Outcome Measures

Arms

Observational (Physical tests, questionnaires, record review)

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

Electronic Health Record Review

Undergo medical record review

Physical Performance Testing

Undergo physical performance testing

Quality-of-Life Assessment

Complete assessments

Questionnaire Administration

Complete questionnaire

Primary outcome measure

  • Functions of patients who underwent internal hemipelvectomy with or without reconstruction or have had an external hemipelvectomy [ Time Frame: Through study completion, average of 1 year ]

Central Contacts and Locations

Central contacts

Valerae O Lewis

713-792-5073volewis@mdanderson.org

Locations

M D Anderson Cancer Center

Recruiting

Houston, Texas, United States, 77030

Contacts

Valerae O. Lewis

713-792-5073

Principal Investigator:

Valerae O. Lewis

More Information

Sponsor

M.D. Anderson Cancer Center

Last update posted

May 20, 2026

Last verified

May, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by M.D. Anderson Cancer Center on 2026-05-20.