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NCT06133647 Clinical Trial

Demographics, Characteristics and Outcomes of Male Breast Cancer Patients at Methodist Health System

Ductal Carcinoma in Situ Clinical Trial

Official title:
Demographics, Characteristics and Outcomes of Male Breast Cancer Patients at Methodist Health System

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06133647
Other study ID # 015.MTP.2023.A
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 4, 2023
Est. completion date May 4, 2024

Study information
Verified date January 2024
Source Methodist Health System
Contact Colette N Ngo Ndjom, MS
Phone 214-947-1280
Email MHSIRB@mhd.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To determine the number of MBC cases as well as the demographics, characteristics, and outcomes of MBC patients at Methodist Health System (MHS).

Description:

Male breast cancer (MBC) is a rare disease without sufficient clinical data supporting the management and treatment. The treatment of MBC arises from data extrapolated from female breast cancer (FBC). MBC has higher mortality than FBC. Previous studies have suggested differences between MBC and FBC; however, treatments remain the same for both. Larger studies in MBC are needed to provide more clinical data to help guide treatment.

Recruitment information / eligibility
Status Recruiting
Enrollment 8
Est. completion date May 4, 2024
Est. primary completion date May 4, 2024
Accepts healthy volunteers
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - • = 18 years of age Patients diagnosed with ductal carcinoma in situ or invasive lobular carcinoma of the breast Exclusion Criteria: - 18 years of age - Prisoners - Pregnant or breastfeeding

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• managing Male Breast Cancer Patients at Methodist Health System
To determine the number of MBC cases as well as the demographics, characteristics, and outcomes of MBC patients at Methodist Health System (MHS).

Locations
Country Name City State
United States Clinical Research Institute at Methodist Health System Dallas Texas
United States Clinical Research Institute at Methodist Health System Dallas Texas

Sponsors (1)
Lead Sponsor Collaborator
Methodist Health System

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Diagnosis Rates of patients with MBC and FBC complications of treatment 13 years
Primary Recurrence rates of Patients with MBC and FBC Recurrence rates of Patients with MBC and FBC 13 years
Primary Duration of remission in Patients with MBC and FBC Duration of remission in Patients with MBC and FBC 13 years
Primary The Overall Survival of patients with MBC and FBC after receiving treatment The Overall Survival of patients with MBC and FBC after receiving treatment 13 years
Primary Determine the complications of Treatment in patients with MBC and FBC Determine the complications of Treatment in patients with MBC and FBC 13 years
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