- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06357338
Differential Expression and Potential Value of c-MYC in Non-Invasive and Invasive Mammary Carcinoma
April 5, 2024 updated by: Marwa Mahmoud Hassan
Differential Expression and Potential Value of c-MYC in Non-invasive and Invasive Mammary Carcinoma
Retrospective observational study to evaluate c-MYC expression in non invasive and invasive mammry carcinoma
Study Overview
Status
Enrolling by invitation
Conditions
Intervention / Treatment
Detailed Description
To correlate different levels of c-MYC expressions with variable clinical and pathological parameters of mammary carcinoma (such as patients' ages, tumor grading, staging, laterality, focality and nodal metastasis, co-existing in-situ components).
This study will be carried out on archived formalin-fixed and paraffin embedded tissue blocks that were belonged to 70 women with breast lumps.
Study Type
Observational
Enrollment (Estimated)
70
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Sohag, Egypt
- Sohag University
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
women with breast lumps administered to oncology center
Description
Inclusion Criteria:
Specimens of Modified Radical Mastectomies from breast carcinoma patients
Exclusion Criteria:
Cases with insufficient clinical data.
- Tissue blocks of destroyed or insufficient material, unfit for diagnosis.
- Cases who received pre-operative chemotherapy.
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
non invasive mammary carcinoma
35 cases with non invasive breast cancer with low and high nuclear grades and co existing microfoci of invasion
|
No intervention
|
|
invasive mammary carcinoma
35 cases of invasive breast cancer undergone MRM and classify them according grading, staging and luminal subtypes
|
No intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
role of c-MYC in breast cancer
Time Frame: 1 year
|
difference between expression of c-MYC in non invasive and invasive mammary carcinoma
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Afaf Alnashar, professor, Sohag University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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 (Actual)
March 19, 2024
Primary Completion (Estimated)
April 1, 2025
Study Completion (Estimated)
April 1, 2026
Study Registration Dates
First Submitted
April 5, 2024
First Submitted That Met QC Criteria
April 5, 2024
First Posted (Actual)
April 10, 2024
Study Record Updates
Last Update Posted (Actual)
April 10, 2024
Last Update Submitted That Met QC Criteria
April 5, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Soh-Med-24-03-15MS
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.