Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Using 68Ga-DOTATATE PET/CT to diagnose soft tissue sarcomas

Official title: Clinical Feasibility and Potential Clinical Benefit of 68Ga-DOTATATE PET/CT Assessment of Soft Tissue Sarcomas for Potential Peptide Receptor Radionuclide Therapy

Run by Ohio State University Comprehensive Cancer Center · NCT06500065 · Data updated 2026-11-12

This study is testing a new type of imaging called 68Ga-DOTATATE PET/CT to see if it can help doctors better diagnose soft tissue sarcomas in patients.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment30 (estimated)
SponsorOhio State University Comprehensive Cancer Center
Academic / other
Drugs / interventionsradiation, chemotherapy
Locations1 site (Columbus, Ohio)
StatusRecruiting
StartedSeptember 30, 2024
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedFebruary 2, 2026
Trial IDNCT06500065 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 18 and older diagnosed with any stage of soft tissue sarcomas who are candidates for systemic therapies.

Probably not a fit

Patients with hypersensitivity to somatostatin, those who have received long-acting somatostatin analogs recently, or those unable to undergo the imaging due to claustrophobia or other medical conditions may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This trial evaluates the effectiveness of 68Ga-DOTATATE digital PET/CT imaging in diagnosing soft tissue sarcomas. The study aims to assess the feasibility and capability of this advanced imaging technique, which may enhance image quality and provide better detection of tumors. Patients will receive the radiotracer intravenously and undergo imaging to evaluate tumor characteristics and response to therapy. The trial also seeks to determine the safety of 68Ga-DOTATATE in this patient population.

Why it matters

Potential benefit: If successful, this approach could lead to more accurate diagnoses and better treatment planning for patients with soft tissue sarcomas.

How similar studies have gone: While this specific approach is novel, similar imaging techniques have shown promise in enhancing diagnostic capabilities for various cancers.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients \>= 18 years of age
* Patients diagnosed with any stage of soft tissue sarcomas candidates for systemic therapies
* Patients with one standard of care PET/CT scan up to 30 days before enrollment at the Ohio State University facilities.

Exclusion Criteria:

* Hypersensitivity to somatostatin or similar peptides
* Somatostatin long-acting analog in the past 6 months
* Patients who are pregnant or lactating
* Patients who are currently incarcerated
* Patients with acute infections
* Inability to complete the needed investigational and standard-of-care imaging examinations due to other reasons (severe claustrophobia, radiation phobia, etc.)
* Patients exceeding the weight limitations of the scanner or are not able to enter the bore of the dPET/CT scanner due to body mass index (BMI)

Where it's running

  • Ohio State University Comprehensive Cancer Center
    Columbus, Ohio, United States
    Recruiting

Study contacts

  • Principal investigator: Gabriel R Tinoco Suarez — Ohio State University Comprehensive Cancer Center

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.