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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02457962
Other study ID # 15-000136
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 2015
Est. completion date April 2025

Study information

Verified date July 2023
Source Mayo Clinic
Contact Clinical Trials Referral Office
Phone 855-776-0015
Email Anderson.Jeffrey@mayo.edu
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

To collect and analyze specimens that will correlate with clinical outcomes such as acute and late toxicities, quality of life, local control, and survival of patients treated with photon/proton therapy.


Recruitment information / eligibility

Status Recruiting
Enrollment 15000
Est. completion date April 2025
Est. primary completion date April 2025
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: 1. Treated with photon/proton at Mayo Clinic Rochester in Radiation Oncology 2. Radiation therapy for curative intent Exclusion Criteria: None

Study Design


Locations

Country Name City State
United States Mayo Clinic Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary analyze acute and late toxicities using CTCAE 4.03 Patients will be followed for the duration of their life, an expected average of 20 years
Primary analyze quality of life using LASA-3 and FACT-E Patients will be followed for the duration of their life, an expected average of 20 years
Secondary analyze local control through tumor assessments Patients will be followed for the duration of their life, an expected average of 20 years
Secondary analyze survival by contacting patient and EMR (electronic medical record) review Patients will be followed for the duration of their life, an expected average of 20 years
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