Recruiting now—Ages 18 Years and up
Recognition of Circulating Tumor DNA in Soft Tissue Sarcoma
Sponsor: Medical College of Wisconsin · NCT03896620 on ClinicalTrials.gov ↗
Conditions studied
Sarcoma
What it tests
- Preoperative RTdevice
- Postoperative RTdevice
- Chemotherapydrug
- Surgeryother
Where it's running1 site
- Recruiting now
Froedtert Hospital & the Medical College of Wisconsin
Milwaukee, Wisconsin 53226
- Meena Bedi, MD(contact)414-805-4400[email protected]
See the official eligibility language
Shown exactly as written on ClinicalTrials.gov. Your oncologist is the right person to judge whether it fits your situation.
Inclusion Criteria: * Have signed an Institutional Review Board (IRB)/Independent Ethics Committee (IEC)-approved informed consent form (ICF) prior to any study-specific evaluation. * Diagnosis of soft tissue sarcoma. * ≥ 18 years of age. * Planned biopsy obtained within four weeks after registration. * History and physical within eight weeks prior to registration. * For stage II-III patients, no prior therapy to primary site of sarcoma. * Computerized tomography (CT), positron emission tomography (PET) /CT or MR imaging of the affected primary site obtained in stage II-III or metastatic site in stage IV patients within eight weeks prior to registration. * CT chest or PET /CT acquired to assess distant disease within eight weeks prior to registration for stage II-III patients. * Karnofsky Performance Scale (KPS) 60 or above within four weeks prior to registration. * Documentation of stage within eight weeks prior to registration. * Biopsy of primary or metastatic disease site must be safe, feasible and in concordance with standard of care per the treating physician and/or radiologist. * Life expectancy ≥ 12 weeks. Exclusion Criteria: * Pregnant women. * Patients with a history of metastatic disease from a primary other than sarcoma. * Patients who cannot undergo imaging as part of treatment planning or surveillance.
Updated 2025-12-24 on ClinicalTrials.gov. Always confirm current details with the study team or your oncologist.