- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06792591
Diagnostic Performance of Positron Emission Mammography in Breast Cancer
January 20, 2025 updated by: Zainab Fathy Mohammed, Assiut University
Investigate the accuracy of PEM in detection of breast cancer.
Study Overview
Detailed Description
Investigate the accuracy of positron emission mammography as non invasive method for early detection of breast cancer especially small sized cancers.
Study Type
Observational
Enrollment (Estimated)
54
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Zainab Fathy Mohammad
- Phone Number: +20 01099024404
- Email: zainab.fathy.95@gmail.com
Study Contact Backup
- Name: Maha Khalil Mahmoud
- Phone Number: +20 10 04037100
- Email: mahakhalil12@yahoo.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
Patients suspected with breast cancer or pathological proven to have breast cancer, patients underwent breast mammography or breast US and suspected to have breast cancer.
Description
Inclusion Criteria:
- patients suspected with breast cancer.
Exclusion Criteria:
- patient with glucose level >200 mg/dl.
- Pregnant patients
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Diagnostic performance of positron emission mammography in breast cancer
Time Frame: Base line
|
Investigate PEM as non invasive method for early detection of breast cancer
|
Base line
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
February 1, 2025
Primary Completion (Estimated)
September 1, 2026
Study Completion (Estimated)
November 1, 2026
Study Registration Dates
First Submitted
January 20, 2025
First Submitted That Met QC Criteria
January 20, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 20, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PEM in breast cancer
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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Northwestern UniversityEisai Inc.UnknownMale Breast Cancer | Stage II Breast Cancer | Stage IIIA Breast Cancer | Stage IIIB Breast Cancer | Triple-negative Breast Cancer | Stage IA Breast Cancer | Stage IB Breast Cancer | Stage IIIC Breast Cancer | Estrogen Receptor-negative Breast Cancer | Progesterone Receptor-negative Breast Cancer | HER2-negative...United States
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