Comparative Study of Sensitivity of Ga-DOTATOC PET vs Octreoscan SPECT + CT
NCT01869725 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 68
Last updated 2021-09-22
Summary
This clinical trial studies gallium Ga 68-edotreotide positron emission tomography (PET)/computed tomography (CT) compared with indium In 111 pentetreotide plus contrast-enhanced CT (or MRI) in diagnosing patients with neuroendocrine tumors and other somatostatin receptor positive tumors. Diagnostic procedures, such as gallium Ga 68-edotreotide PET/CT, may help find and diagnose somatostatin receptor positive neuroendocrine tumors. It is not yet known whether Ga 68-edotreotide PET/CT is as effective as indium In 111 pentetreotide plus contrast-enhanced CT (or MRI) in diagnosis and staging of patients with neuroendocrine tumors.
Conditions
- Adult Medulloblastoma
- Childhood Medulloblastoma
- Neuroblastoma
- Neuroendocrine Tumor
- Somatostatinoma
Interventions
- DRUG
-
gallium Ga 68-edotreotide
Given IV
- PROCEDURE
-
positron emission tomography/computed tomography
Undergo gallium Ga 68-edotreotide PET/CT scan
- RADIATION
-
indium In 111 pentetreotide
Undergo indium In 111 pentetreotide contrast-enhanced CT or MRI scan
- PROCEDURE
-
computed tomography
Undergo indium In 111 pentetreotide contrast-enhanced CT scan
- PROCEDURE
-
contrast-enhanced magnetic resonance imaging
Undergo indium In 111 pentetreotide contrast-enhanced CT or MRI scan
Sponsors & Collaborators
-
National Cancer Institute (NCI)
collaborator NIH -
Sue O'Dorisio
lead OTHER
Principal Investigators
-
M. Sue O' Dorisio, MD, PhD · University of Iowa
Study Design
- Allocation
- NA
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 2 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-04-01
- Primary Completion
- 2018-12-26
- Completion
- 2018-12-26
- FDA Drug
- Yes
Countries
- United States
Study Locations
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