Neuroendocrine Tumors Clinical Trial
— PET/Ga68Official title:
Phase II Study to Measure the Safety of 68Ga-DOTA-TATE PET/CT in the Diagnosis of Tumors Expressing Somatostatin Receptors
Phase-II, prospective, open label, no control group to assess the safety of 68Ga-DOTA-TATE injection in patients with suspected or diagnosed with tumors expressing somatostatin receptors. Each included patient will receive an administered dose of 50 mcg or less of the peptide (DOTA-TATE) and a range of activity between 100 - 200 MBq of 68Ga-DOTA-TATE. The efficacy of 68Ga-DOTA-TATE in assessing this kind of tumors has been proved by numerous studies.
Status | Completed |
Enrollment | 2120 |
Est. completion date | May 29, 2020 |
Est. primary completion date | January 1, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility | Inclusion Criteria: 1. Patients with suspected or proven tumors expressing Somatostatin receptors 2. Informed consent by patient (or parents if patient is less than 18 years of age) Exclusion Criteria: 1. Pregnancy (confirmed). In the case of a diagnostic procedure in a patient who is or may be pregnant, a clinical decision is necessary considering the benefits against the possible harm of carrying out any procedure. 2. Patient refusal to participate. 3. Impossibility to tolerate a decubitus position for 25 minutes 4. Prior allergic reaction to DOTA-TATE or somatostatin analogs |
Country | Name | City | State |
---|---|---|---|
Canada | Centre hospitalier universitaire de Sherbrooke | Sherbrooke | Quebec |
Lead Sponsor | Collaborator |
---|---|
Centre de recherche du Centre hospitalier universitaire de Sherbrooke |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Record all adverse events | June 2016-June 2018 |
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