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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01694225
Other study ID # BCC-BRE-12-Adherence
Secondary ID
Status Completed
Phase N/A
First received September 23, 2012
Last updated January 29, 2018
Start date July 2012
Est. completion date January 28, 2018

Study information

Verified date December 2017
Source University of Louisville
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to establish the feasibility of using a monthly bubble package to improve compliance rates among women prescribed adjuvant endocrine therapy.


Description:

This study uses Bubble packaging to provide a cost effective way to improve compliance and help direct further interventions to ensure adherence in women on anti-estrogen therapy for breast cancer.


Recruitment information / eligibility

Status Completed
Enrollment 87
Est. completion date January 28, 2018
Est. primary completion date January 28, 2018
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years of age or older

- Estrogen receptor positive (> 1% estrogen expression) by immunohistochemistry

- Invasive breast cancer (stage I, II, III) or DCIS considered for adjuvant endocrine therapy

Exclusion Criteria:

- Patients with metastatic disease (stage IV)

- Patients less than 18 years of age

- Prisoners

- Patients are unable to fill prescriptions at the BCC pharmacy due to insurance limitations or personal preference

Study Design


Related Conditions & MeSH terms


Intervention

Other:
bubble packaging for monthly prescription
Monthly bubble packaging among women prescribed anti-estrogens

Locations

Country Name City State
United States James Graham Brown Cancer Center-University of Louisville Louisville Kentucky

Sponsors (2)

Lead Sponsor Collaborator
University of Louisville James Graham Brown Cancer Center

Country where clinical trial is conducted

United States, 

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