Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Pennsylvania
Age
40–70
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Written informed consent was obtained and documented (after the investigator has given oral and written information about the study to the subject).
The subject was conscious, co-operative, and agreed to return for the scheduled visits and tests and any visits required to obtain additional safety information.
The subject's medical history, physical examination (including vital signs, pulse oximetry, PFT's, and 12-lead electrocardiogram \[ECG\]), and clinical laboratory tests (hematology, serum chemistry) obtained at the screening visit were within acceptable limits for entry into the study, as judged by the investigator.
You may not be if
Subject is \<40 or \>70 years old
Subject known to be pregnant
Subject with a baseline oxygen requirement \> 2 l/min via nasal cannula
Any known contraindication to MRI examination
Inability to provide informed consent
A language, communication, cognitive or behavioral impairment that might interfere with fully informed consent
Active drug or alcohol dependence
Homelessness or other unstable living situation
Active drug or alcohol dependence
Significant co-morbidities such as heart disease, kidney disease, liver disease, hematologic or neurological disease that require continuing treatment.