Status:
COMPLETED
Hyperpolarized Xenon MRI for Assessment of Pulmonary Function in Lung Resection
Lead Sponsor:
Polarean, Inc.
Conditions:
Pulmonary Surgical Procedures
Eligibility:
All Genders
18+ years
Phase:
PHASE3
Brief Summary
This study compares the equivalence of hyperpolarized 129Xe MRI as compared to 133Xe scintigraphy for the evaluation of pulmonary function in patients being evaluated for lung resection.
Detailed Description
This is a multicenter, randomized, open-label, cross-over Phase 3 study evaluating hyperpolarized 129Xe gas MRI as compared to 133Xe scintigraphy for the evaluation of pulmonary function. This study w...
Eligibility Criteria
Inclusion
- Male or female subjects ≥18 years of age.
- Subject is being evaluated for possible lung resection (e.g., segmentectomy, lobectomy, or pneumonectomy).
- Subject is able to undergo MRI imaging and able to fit in the MRI coil.
- Subject is willing and able to comply with all study procedures.
- Subject must understand and voluntarily sign an informed consent form (ICF) prior to any study specific assessments or procedures.
Exclusion
- Baseline blood oxygen saturation (SpO2) \<90% at rest. For patients requiring routine supplemental oxygen, SpO2 measurements should be taken with the patient's normal oxygen supplementation.
- Female subjects of childbearing potential with a positive serum pregnancy test at screening, or who are not taking (or not willing to take) acceptable birth control measures through the Follow-up Period. Adequate birth control methods include with a monogamous partner who was sterilized more than 6 months prior to screening, or measures with a Pearl index of \<1 used consistently and correctly (including intrauterine devices, or implantable, injectable, oral, or transdermal contraceptives). Women are not considered to be of childbearing potential if they meet at least 1 of the following 2 criteria as documented by the Investigator:
- They have had a hysterectomy, bilateral salpingectomy, or bilateral oophorectomy at a minimum of 1 menstrual cycle prior to signing the ICF; or
- They are post-menopausal: for women ≥55 years of age, defined as ≥1 year since their last menstrual period, or for women \<55 years of age, defined as ≥1 year since their last menstrual period and have a follicle-stimulating hormone (FSH) level in the laboratory's normal range for post-menopausal phase.
- Women who are lactating and insist on breast feeding.
- Subjects who have received any other investigational therapy within 4 weeks prior to Screening.
- Subjects who require anesthesia or heavy sedation to undergo MRI testing. Mild sedation could be acceptable (i.e. a low dose oral acting anxiolytic medication such as alprazolam) as long as, in the opinion of the investigator, the subject meets Inclusion Criteria #4 and #5.
Key Trial Info
Start Date :
August 17 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 10 2020
Estimated Enrollment :
38 Patients enrolled
Trial Details
Trial ID
NCT03417687
Start Date
August 17 2018
End Date
March 10 2020
Last Update
June 28 2022
Active Locations (3)
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1
Duke University Hospital
Durham, North Carolina, United States, 27710
2
University of Cincinnati Medical Center
Cincinnati, Ohio, United States, 45219
3
University of Virginia
Charlottesville, Virginia, United States, 22908