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Clinical Trials/NCT03128710
NCT03128710
Completed
Not Applicable

Identifying Patient-relevant Adverse Events Following Prostate Radiotherapy

University of Maryland, Baltimore1 site in 1 country224 target enrollmentMarch 15, 2017
ConditionsProstate Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
University of Maryland, Baltimore
Enrollment
224
Locations
1
Primary Endpoint
To determine patient preference weights for side effect reduction in radiation treatment of prostate cancer
Status
Completed
Last Updated
last year

Overview

Brief Summary

There have been calls from patients, payers, healthcare providers, and policy makers for an evaluation of newer, high-cost radiation technologies compared to conventional forms of radiation therapy. National attention has focused on the use of intensity modulated radiation therapy (IMRT) into routine daily clinical practice for prostate cancer. The goal of the present study is to determine whether the type of radiation treatment received by the patients can result in a reduction in patient-relevant side effects following prostate irradiation. The analysis will be performed by obtaining patient answered surveys looking at side effects.

Registry
clinicaltrials.gov
Start Date
March 15, 2017
End Date
February 15, 2018
Last Updated
last year
Study Type
Observational
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Department of Radiation Oncology

Principal Investigator

University of Maryland, Baltimore

Eligibility Criteria

Inclusion Criteria

  • Participant is 18 years or older
  • Has been diagnosed with prostate cancer
  • Able to speak and read English

Exclusion Criteria

  • Participant is not being seen for prostate cancer
  • Under the age of 18

Outcomes

Primary Outcomes

To determine patient preference weights for side effect reduction in radiation treatment of prostate cancer

Time Frame: 3 years

Investigators will use an anonymous survey and results from multiple focus groups to quantify the relative importance/significance of commonly encountered side effects experienced by patients following external beam radiation therapy. We will complete descriptive statistics as a means of understanding the data obtained by survey responses. Additionally, comparative analyses may be undertaken to evaluate differences between different side effects experienced.

Study Sites (1)

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