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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00903890
Other study ID # ULYM07056
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 2008
Est. completion date April 9, 2020

Study information

Verified date August 2023
Source University of Rochester
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is to inquire by mailed survey regarding the cardiac and general health of patients previously treated for Hodgkin's and non-Hodgkin's lymphoma with radiation therapy/anthracycline chemotherapy.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date April 9, 2020
Est. primary completion date November 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - All patients with Hodgkin's Lymphoma and Non Hodgkin's lymphoma who underwent Radiation Therapy (RT) to either a mantle or modified mantle field with or without adriamycin at the Wilmot Cancer Center at the University of Rochester are eligible for the study. Exclusion Criteria: - Any severe preexisting cardiac disease (e.g., arrhythmia, angina, coronary disease, myocardial infarction, or congestive heart failure) prior to diagnosis

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Survey
Survey asking questions regarding the subjects cardiac and general health.

Locations

Country Name City State
United States University of Rochester Medical Center Rochester New York

Sponsors (1)

Lead Sponsor Collaborator
University of Rochester

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measure changes in Cardiac ejection fraction score Post Radiation Treatment
Primary Measure changes in perfusion imaging score on the radionuclide cardiac profusion scan Post Radiation
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