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NCT02613312 Clinical Trial

Chemotherapy Followed by Surgery and Neoadjuvant Hemothoracic Intensity Modified Radiation Therapy (IMRT) for Patients With Malignant Pleural Mesothelioma

Mesothelioma Clinical Trial

Official title:
Chemotherapy Followed by Surgery and Neoadjuvant Hemothoracic Intensity Modified Radiation Therapy (IMRT) for Patients With Malignant Pleural Mesothelioma

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02613312
Other study ID # 15-007645
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 18, 2016
Est. completion date December 2024

Study information
Verified date April 2024
Source Mayo Clinic
Contact Karlyn Pierson, RN
Phone 507-293-0807
Email pierson.karlyn@mayo.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine the response rate and overall survival in patients that have been diagnosed with mesothelioma and will undergo chemotherapy, surgery and intensity modified radiation therapy (IMRT) as part of their standard of care.

Description:

The investigators will consent patients that have been diagnosed with mesothelioma and will undergo chemotherapy followed by surgery and then IMRT as their standard of care. The investigators will collect data from past and future medical records as well as data regarding their health status for their lifetime by reviewing life status, treatment status and CT scans.

Recruitment information / eligibility
Status Recruiting
Enrollment 200
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Subject provides informed consent - Subject is >18 years of age - Subject is deemed competent for making medical decisions - Subject is scheduled to undergo chemotherapy followed by surgery and then IMRT - Subject is a surgical candidate - A negative pregnancy test is required in women of child-bearing potential, as standard of care. Exclusion Criteria: •Subject is <18 years old.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Mayo Clinic in Rochester 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 Survival status upon review of patients every 6 months 2 years
Secondary Progression free survival as evidenced by CT scan review 2 years
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