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Staging Procedures to Diagnose Malignant Pleural Mesothelioma

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ClinicalTrials.gov Identifier: NCT02648763
Recruitment Status : Recruiting
First Posted : January 7, 2016
Last Update Posted : February 6, 2019
Sponsor:
Information provided by (Responsible Party):
Dennis Wigle, Mayo Clinic

Brief 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.

Condition or disease
Mesothelioma Solitary Fibrous Tumor of the Pleura

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Study Type : Observational
Estimated Enrollment : 200 participants
Observational Model: Case-Only
Time Perspective: Prospective
Official Title: Staging Procedures to Diagnose Malignant Pleural Mesothelioma
Actual Study Start Date : March 14, 2016
Estimated Primary Completion Date : December 2020
Estimated Study Completion Date : December 2020

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Mesothelioma




Primary Outcome Measures :
  1. Accuracy of surgical staging versus imaging procedures based on surgical findings. [ Time Frame: 2 years ]
    The staging imaging will be compared with the actual surgical staging procedure to evaluate the accuracy of the imaging.



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients receiving treatment at the Mayo Clinic Rochester 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.
Criteria

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.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02648763


Contacts
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Contact: Karlyn Pierson, RN 507-293-0807 pierson.karlyn@mayo.edu
Contact: Bettie Lechtenberg, MBA 507-293-0807 lechtenberg.bettie@mayo.edu

Locations
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United States, Minnesota
Mayo Clinic in Rochester Recruiting
Rochester, Minnesota, United States, 55905
Contact: Karlyn E Pierson, RN    507-538-1960    pierson.karlyn@mayo.edu   
Principal Investigator: Dennis A Wigle, MD, PhD         
Sponsors and Collaborators
Mayo Clinic
Investigators
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Principal Investigator: Dennis Wigle, MD, PhD Mayo Clinic

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Responsible Party: Dennis Wigle, Principal Investigator, Mayo Clinic
ClinicalTrials.gov Identifier: NCT02648763     History of Changes
Other Study ID Numbers: 15-007647
First Posted: January 7, 2016    Key Record Dates
Last Update Posted: February 6, 2019
Last Verified: February 2019

Additional relevant MeSH terms:
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Mesothelioma
Solitary Fibrous Tumors
Neoplasms, Fibrous Tissue
Solitary Fibrous Tumor, Pleural
Pleural Neoplasms
Adenoma
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Neoplasms
Neoplasms, Mesothelial
Neoplasms, Connective Tissue
Neoplasms, Connective and Soft Tissue
Respiratory Tract Neoplasms
Thoracic Neoplasms
Neoplasms by Site
Pleural Diseases
Respiratory Tract Diseases