Comparing Ga-68-DOTATATE and Ga-68-DOTATOC for Meningioma

This study is comparing two imaging agents, Ga-68-DOTATATE and Ga-68-DOTATOC, used in PET scans (a type of imaging test) for patients with meningioma (a type of brain tumor). The goal is to see which agent provides clearer images of the tumor compared to surrounding brain tissue. Researchers want to find out if Ga-68-DOTATOC is as good as Ga-68-DOTATATE, potentially leading to a more cost-effective imaging method. You may be able to join if you are an adult with suspected meningioma, are planning to have surgery, and have no reasons preventing you from receiving these imaging agents. The study aims to measure how well each agent highlights the tumor visually and quantitatively. The current recruitment status is unclear.

Study design
This interventional study plans to enroll 6 participants. It directly compares two different imaging agents.
What's involved
You would undergo two PET scans using the different imaging agents. You must be able to lie still on the scanner table for the required time.
Compensation
Not stated in the trial record.
Follow-up
The primary outcomes will be measured over 12 months.

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NCT04298541

Direct Comparison of Ga-68-DOTATATE and Ga-68-DOTATOC

Not Yet Recruiting
PHASE2Ages 18–89InterventionalDiagnostic
Weill Medical College of Cornell University
~6 participants
Updated 2026-02-27 on ClinicalTrials.gov
What's tested:Ga-68- DOTATATEGa-68-DOTATOC

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Qualitatively measure the visual appearance of target lesion to cranial blood pool using the maximum SUV ratio to compare results from Ga-68-DOTATATE and -DOTATOC PET.
Measured over Over 12 months
+1 more outcome measured
Meningioma
1 sites across 1 states
New York1
  • Jana Ivanidze, MD/Ph.D · PRINCIPAL_INVESTIGATOR · Weill Medical College of Cornell University

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Eligibility criteria

Inclusion

Adult patients with clinically suspected meningioma
Patients planned for surgery - undergoing preoperative workup
No contraindications to either radiotracer

Exclusion

Age less than 18 years
Inability to lay on the scanner table for the required period of time, e.g., due to bone pain or claustrophobia.
  • Qualitatively measure the visual appearance of target lesion to cranial blood pool using the maximum SUV ratio to compare results from Ga-68-DOTATATE and -DOTATOC PET.Over 12 months

    Compare visual appearance qualitatively using the maximum SUV ratio of target lesion to cranial blood pool (i.e. superior sagittal sinus reference region) of DOTATATE and DOTATOC PET scans in patients with meningioma. Based on our pilot clinical case series, the following reference regions will be evaluated: 1. Suspected meningioma; 2. Pituitary gland; 3. Superior sagittal sinus; 4. Brain parenchyma. Dynamic PET will be acquired and data will be analyzed including comparison of tissue-activity curves and Patlak analysis, as established by the PI in a pilot cohort. Extent of meningioma based on Ga-68-DOTATATE- and DOTATOC PET/CT will be compared to extent of disease as determined by MRI.

  • Quantitatively measure the visual appearance of target lesion to cranial blood pool using the maximum SUV ratio to compare results from Ga-68-DOTATATE and -DOTATOC PET.Over 12 months

    Compare visual appearance quantitatively using the maximum SUV ratio of target lesion to cranial blood pool (i.e. superior sagittal sinus reference region) of DOTATATE and DOTATOC PET scans in patients with meningioma. Qualitative analysis will include evaluation by board certified radiologists with expertise in nuclear medicine/ molecular imaging who will be blinded to the radiotracer injected. Quantitative analysis will include extraction of the ratio of lesion's SUVmax values/reference regions.