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RecruitingNCT07215611Updated Sep 11, 2026

Financial Toxicity in Patients With Resected Soft Tissue and Bone Sarcomas

An observational study in Bone Sarcomas and Financial Toxicity, sponsored by M.D. Anderson Cancer Center. Recruiting at 1 site in United States. Per ClinicalTrials.gov, last updated 2026-09-11.

Sponsored by M.D. Anderson Cancer Center · Observational

From the registry’s dates

  • Started Sep 2025; still recruiting 1 year 2 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Sex
All
01

Study summary

To learn about the financial stress patients undergoing surgery to treat orthopedic cancer experience because of the costs of cancer care, and to learn about the effects of financial stress on participants quality of life.

Read the detailed description

Measure the prevalence of financial toxicity and the severity of it in orthopaedic oncology patients undergoing surgical intervention using an objective, validated instrument. Secondary objectives include identifying socioeconomic and demographic risk factors for financial toxicity and evaluating clinicopathologic characteristics that may worsen financial stress in this population.

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Conditions studied

  • Bone Sarcomas
  • Financial Toxicity
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In context

Bone Neoplasms

258 studies on the registry are indexed under Bone Neoplasms; 68 are open to participants now.

This study's planned enrollment of 100 is close to the median of 101 across 82 observational studies indexed under Bone Neoplasms.

Browse Bone Neoplasms studies →

Lead sponsor

M.D. Anderson Cancer Center is the lead sponsor of 3,047 studies on the registry; 578 are open to participants now.

Of its 612 completed or terminated interventional studies of FDA-regulated products, 409 (67%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

MD Anderson Cancer Center

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Participants who are seen preoperatively at our institution before surgery for primary malignant bone tumor or primary malignant soft tissue tumor will be identified.
  • Adult orthopedic oncology patients. Stratified by diagnosis of primary malignant bone tumor and primary malignant soft tissue tumor.

Exclusion criteria

Exclusion Criteria

  • Non-English subjects will not be recruited. Subjects are required to be able to read/write in English.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No

Interventions

  • Otherdata collection

    data collection from electronic health records

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What researchers measure

Primary outcomes

  1. Questionnaires

    Time frame: Through study completion; an average of 1 year

07

Study locations

1 of 1 sites recruiting
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References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07215611
Responsible party
Sponsor
First posted
Oct 10, 2025
Start date
Sep 2, 2025
Primary completion
Oct 2, 2028 (estimated)
Completion
Oct 2, 2030 (estimated)
Last update
Sep 11, 2026

Study contacts

Shalin S Patel, MD
Contact
sspatel@mdanderson.org
713-792-6268
Shalin S Patel, MD
principal investigator · M.D. Anderson Cancer Center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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