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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05141279
Other study ID # CESM in breast cancer
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date December 1, 2021
Est. completion date January 1, 2024

Study information

Verified date November 2021
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this work to evaluate the accuracy of contrast enhanced spectral mamography in predicting the response to NAC and assessment of residual disease in breast cancer patients


Description:

This a prospective series ,will be performed for 50 patients diagnosed by biopsy as breast cancer who will be scheduled for surgery after completing the full coarse of neoadjuvant chemotherapy


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date January 1, 2024
Est. primary completion date December 1, 2023
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - patient confirmed diagnosed by early breast cancer decided to received neoadjuvant treatment - locally advanced breast cancer - operable metastatic breast cancer Exclusion Criteria: - patient not candidate for NAC - contrast allergy - renal impairment - pregnancy

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary Accuracy of contrast enhanced spectral mamography in the predicting of pathological response to NAC and assessment residual disease in breast cancer patients Basline
Secondary Assess best imaging modalities in pedict post neoadjuvant response Baseline
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