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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02648763
Other study ID # 15-007647
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 14, 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 evaluate the accuracy of participants imaging versus staging procedures. The investigators will consent subjects that are scheduled to undergo staging procedures to diagnose malignant pleural mesothelioma (including pleuroscopy, bronchoscopy, endobronchial ultrasound and laparoscopy) as part of their standard of care.


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 a staging pleuroscopy - 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 Accuracy of surgical staging versus imaging procedures based on surgical findings. The staging imaging will be compared with the actual surgical staging procedure to evaluate the accuracy of the imaging. 2 years
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