200 Participants Needed

Hemipelvectomy for Pelvic Cancer

VO
Overseen ByValerae O Lewis
Age: Any Age
Sex: Any
Trial Phase: Academic
Sponsor: M.D. Anderson Cancer Center
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to understand how different types of hemipelvectomy surgeries affect individuals with pelvic tumors over the long term. Researchers will assess the impact of these surgeries on daily function and quality of life by examining medical records, physical performance, and patient feedback. Individuals who have had or will undergo a hemipelvectomy (a surgery where part of the pelvis is removed) may be suitable for this study. Participants will undergo tests and complete questionnaires before surgery, a few weeks after, and regularly for up to ten years. As an unphased study, this trial offers a unique opportunity to contribute valuable insights that could enhance future surgical outcomes and quality of life for others.

Do I need to stop my current medications for this trial?

The trial information does not specify whether you need to stop taking your current medications.

Why are researchers excited about this trial?

Researchers are excited about this trial because it offers a comprehensive approach to understanding the long-term effects of hemipelvectomy on quality of life. Unlike standard treatments that focus solely on the surgical outcomes for pelvic tumors, this trial includes regular physical performance tests, quality-of-life assessments, and detailed questionnaires over a span of 10 years. This method aims to capture a holistic view of a patient's recovery journey, providing valuable insights into both physical and emotional well-being post-surgery. By tracking these aspects over time, researchers hope to improve post-operative care and support for patients undergoing this significant procedure.

Who Is on the Research Team?

VO

Valerae O Lewis

Principal Investigator

M.D. Anderson Cancer Center

Are You a Good Fit for This Trial?

Inclusion Criteria

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

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Pre-surgery Assessment

Participants undergo physical performance assessments and complete quality of life assessments and questionnaires before hemipelvectomy

1-2 weeks

Post-surgery Assessment

Participants complete quality of life assessments and questionnaires at 6 weeks post-hemipelvectomy

6 weeks

Follow-up

Participants are monitored every 3 months up to 12 months and yearly thereafter for 10 years

10 years

What Are the Treatments Tested in This Trial?

Interventions

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

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Observational (Physical tests, questionnaires, record review)Experimental Treatment4 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

M.D. Anderson Cancer Center

Lead Sponsor

Trials
3,107
Recruited
1,813,000+

National Cancer Institute (NCI)

Collaborator

Trials
14,080
Recruited
41,180,000+