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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT01368939 |
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Date of registration:
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07/06/2011 |
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Primary sponsor: |
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Public title:
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Investigation of High Resolution Nuclear Breast Imaging Camera (MBI) in Patients Administered Tc-99m Sestamibi (ROSE)
ROSE |
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Scientific title:
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A Pilot, Single Centre, Prospective Clinical Study Investigation of the Acceptability of a Dedicated High Resolution Nuclear Breast Imaging Camera (MBI) in Breast Imaging of Patients Administered Tc-99m Sestamibi (ROSE) |
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Date of first enrolment:
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March 2012 |
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Target sample size:
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150 |
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Recruitment status: |
Recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT01368939 |
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Study type:
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Observational |
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Study design:
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Observational Model: Cohort, Time Perspective: Prospective
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Countries of recruitment
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Canada
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Contacts
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Name:
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Tammy Murray, Research Officer |
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Address:
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Telephone:
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905-522-1155 |
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Email:
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tmurray@stjosham.on.ca |
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Affiliation:
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Name:
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Tammy Murray |
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Address:
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Telephone:
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905-522-1155 |
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Email:
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tmurray@stjosham.on.ca |
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Affiliation:
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Name:
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Amit Singnurkar, MD, FRCPC |
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Address:
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Telephone:
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Email:
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Affiliation:
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HHSC, McMaster University, St. Joseph's Healthcare |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- females over 18 years of age
- completed a cardiac stress test using Tc-99m Sestamibi as the radiotracer prior to
MBI imaging on the same day.
- signed consent form
Exclusion Criteria:
- pregnant or lactating
- history of invasive breast cancer or ductal carcinoma in situ
- prior bilateral mastectomy
- prior breast biopsy or surgery within 3 months
- any other conditions that based on the investigator's judgement, may impact the
ability of the patient to complete the study
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Breast Lesions
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Secondary ID(s)
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HHSC-CPDC-001
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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